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EBI Dbfetch

ID   KF456986; SV 1; linear; genomic DNA; STD; HUM; 137 BP.
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AC   KF456986;
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DT   30-JUL-2013 (Rel. 117, Created)
DT   30-JUL-2013 (Rel. 117, Last updated, Version 1)
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DE   Homo sapiens chromosome 20 WGS contig WGS_CHB_AL109911.47_95696 genomic
DE   sequence.
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KW   ASSEMBLY_CORRECTION.
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OS   Homo sapiens (human)
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
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RN   [1]
RP   1-137
RG   Genome Reference Consortium
RA   ;
RT   ;
RL   Submitted (26-JUL-2013) to the INSDC.
RL   NCBI, NIH, Bethesda, MD 20892, USA
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DR   MD5; 48544cdf2f226828f8cd21bb52c8a881.
DR   ENA-CON; GL000143.
DR   ENA-CON; KI270869.
DR   Ensembl-Scaffolds; KF456986.1:1-137; homo_sapiens.
DR   GOA; V9GY03.
DR   GOA; V9GY14.
DR   HGNC; HGNC:11537; TAF4.
DR   InterPro; IPR003894; TAFH_NHR1.
DR   InterPro; IPR007900; TAF4.
DR   UniProtKB/TrEMBL; V9GY03; V9GY03_HUMAN.
DR   UniProtKB/TrEMBL; V9GY14; V9GY14_HUMAN.
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CC   This sequence was generated to audit a questionable region in the
CC   reference genome sequence. This sequence was assembled from a
CC   random sampling of Illumina and LS454 reads representing a single
CC   population of the 1000 Genomes Project
CC   (http://www.1000genomes.org/), using cortex_con
CC   (http://cortexassembler.sourceforge.net/).
CC   ##Metadata-START##
CC   1000 Genomes Population :: CHB
CC   Target                  :: AL109911.47
CC   Target Base             :: 95712
CC   Average Coverage        :: 58.17x
CC   Minimum Coverage        :: 21x
CC   Maximum Coverage        :: 117x
CC   ##Metadata-END##
CC   ##Assembly-Data-START##
CC   Assembly Method       :: cortex_con Beta 0.04c, April 2011
CC   Sequencing Technology :: Illumina GAIIx; 454
CC   ##Assembly-Data-END##
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FH   Key             Location/Qualifiers
FH
FT   source          1..137
FT                   /organism="Homo sapiens"
FT                   /chromosome="20"
FT                   /mol_type="genomic DNA"
FT                   /pop_variant="CHB"
FT                   /clone="WGS_CHB_AL109911.47_95696"
FT                   /db_xref="taxon:9606"
FT   misc_feature    77
FT                   /note="Region: Target update"
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SQ   Sequence 137 BP; 5 A; 20 C; 60 G; 52 T; 0 other;
     gtgggtttga tgtctcctct ccggtgggtg tgggttgtgt gggtttggtg tctcctatcg        60
     ggtggggtgt gggtttgatg tctcctctcg ggtggggtgt gagtttggtg tctcctctcg       120
     ggtgggtgtg ggtttga                                                      137
//


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