A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631757



Internal ID7018566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34984496..34990745hg38UCSC Ensembl
Innerchr13:34984497..34990745hg38UCSC Ensembl
Outerchr13:34984496..34990746hg38UCSC Ensembl
chr13:35558633..35564882hg19UCSC Ensembl
Innerchr13:35558634..35564882hg19UCSC Ensembl
Outerchr13:35558633..35564883hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg386250
hg196250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14688337, essv14688345, essv14688364, essv14688317, essv14688301, essv14688288, essv14688331, essv14688305, essv14688262, essv14688363, essv14688349, essv14688335, essv14688333, essv14688299, essv14688273, essv14688359, essv14688322, essv14688306, essv14688368, essv14688353, essv14688347, essv14688291, essv14688360, essv14688266, essv14688325, essv14688260, essv14688289, essv14688296, essv14688338, essv14688304, essv14688324, essv14688294, essv14688307, essv14688295, essv14688361, essv14688339, essv14688357, essv14688269, essv14688354, essv14688313, essv14688332, essv14688311, essv14688276, essv14688314, essv14688315, essv14688367, essv14688267, essv14688358, essv14688312, essv14688282, essv14688350, essv14688320, essv14688351, essv14688336, essv14688285, essv14688271, essv14688340, essv14688259, essv14688326, essv14688334, essv14688272, essv14688346, essv14688281, essv14688261, essv14688365, essv14688342, essv14688278, essv14688318, essv14688310, essv14688274, essv14688309, essv14688297, essv14688263, essv14688258, essv14688283, essv14688284, essv14688286, essv14688268, essv14688300, essv14688290, essv14688277, essv14688270, essv14688323, essv14688275, essv14688366, essv14688298, essv14688292, essv14688355, essv14688316, essv14688308, essv14688343, essv14688330, essv14688341, essv14688352, essv14688264, essv14688362, essv14688329, essv14688265, essv14688257, essv14688279, essv14688356, essv14688303, essv14688344, essv14688287, essv14688328, essv14688327, essv14688321, essv14688280, essv14688348, essv14688302, essv14688369, essv14688319, essv14688293
SamplesNA20874, HG03857, HG01402, HG01521, HG01918, HG03965, NA12273, HG00358, NA20783, HG04060, HG01537, HG03767, NA21100, NA11933, HG02661, NA21092, NA12045, HG04002, NA12004, NA19684, HG04164, HG00179, HG03792, HG01518, HG00341, HG00150, HG02734, NA20771, HG03679, NA12413, HG00327, HG00272, HG03706, HG03976, HG00173, HG03937, HG03673, HG04182, NA20768, NA19771, NA12287, NA21108, HG04070, NA21103, HG00334, HG03762, NA19923, NA12282, HG03887, HG03619, HG04183, HG00120, NA20278, HG00335, HG00262, HG00232, HG04106, NA18748, HG01284, HG03696, HG03624, NA19722, NA20884, NA20587, HG00264, NA10847, HG00313, HG00266, HG02233, HG01670, HG03644, HG01669, NA12003, HG02697, HG00360, HG01789, HG00368, NA12234, HG03823, HG00740, NA20525, HG00284, NA20867, HG02494, HG00350, NA12829, HG04155, HG01791, HG00117, NA12827, HG03672, NA12778, NA20542, HG00258, NA20799, HG04134, HG03790, HG00357, HG02651, HG03488, NA20504, HG03846, HG03779, HG01765, HG03646, NA20582, HG01085, NA21133, NA20807, HG01781, HG00252, NA20503, HG01695
Known GenesNBEA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631757
Frequency
Sample Size2504
Observed Gain0
Observed Loss113
Observed Complex0
Frequencyn/a


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