A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626870



Internal ID7013700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76431237..76437516hg38UCSC Ensembl
Innerchr11:76431287..76437442hg38UCSC Ensembl
Outerchr11:76431019..76437734hg38UCSC Ensembl
chr11:76142281..76148560hg19UCSC Ensembl
Innerchr11:76142331..76148486hg19UCSC Ensembl
Outerchr11:76142063..76148778hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg386280
hg196280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214176, essv14214166, essv14214168, essv14214155, essv14214174, essv14214193, essv14214209, essv14214217, essv14214199, essv14214175, essv14214162, essv14214205, essv14214186, essv14214138, essv14214184, essv14214142, essv14214135, essv14214147, essv14214172, essv14214165, essv14214152, essv14214187, essv14214131, essv14214202, essv14214179, essv14214153, essv14214173, essv14214203, essv14214206, essv14214213, essv14214216, essv14214180, essv14214177, essv14214215, essv14214181, essv14214129, essv14214197, essv14214136, essv14214200, essv14214137, essv14214171, essv14214192, essv14214208, essv14214212, essv14214201, essv14214154, essv14214195, essv14214178, essv14214161, essv14214160, essv14214191, essv14214207, essv14214188, essv14214167, essv14214196, essv14214148, essv14214169, essv14214146, essv14214211, essv14214144, essv14214204, essv14214134, essv14214159, essv14214194, essv14214214, essv14214190, essv14214210, essv14214183, essv14214145, essv14214133, essv14214170, essv14214158, essv14214140, essv14214143, essv14214198, essv14214132, essv14214150, essv14214185, essv14214141, essv14214139, essv14214163, essv14214149, essv14214130, essv14214189, essv14214182, essv14214156, essv14214164, essv14214157, essv14214151
SamplesHG03514, HG03366, HG02628, NA18508, HG01885, HG02870, HG02323, HG03521, HG03295, HG03172, NA19920, NA19107, HG00641, HG03464, HG03135, HG02840, HG02756, NA19916, HG02645, NA19904, NA19404, HG02562, NA19923, HG02561, NA19383, HG02315, HG02461, NA19238, HG02885, HG03195, HG02642, NA19385, NA19172, NA19471, HG02471, NA19036, HG02882, NA19200, HG02819, HG02009, HG02442, NA19437, HG03088, NA19152, NA18516, HG03428, HG02953, HG02508, HG02968, HG00551, HG01889, NA18907, HG03571, HG03024, NA19099, HG03046, HG03354, HG02330, HG02282, HG02557, HG03240, HG02799, NA20276, NA19712, HG03458, HG00638, NA19428, HG02839, HG03419, NA19818, NA19328, NA18501, HG02971, HG03157, NA19438, HG03097, HG02053, NA19185, HG02768, NA19102, HG03401, HG03445, HG01464, NA19316, HG02465, NA18522, HG03129, HG03439, HG03196
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626870
Frequency
Sample Size2504
Observed Gain0
Observed Loss89
Observed Complex0
Frequencyn/a


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