A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625102



Internal ID7011941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1157818..1163296hg38UCSC Ensembl
chr11:1151445..1156913hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg385479
hg195469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13992411, essv13992388, essv13992344, essv13992367, essv13992365, essv13992357, essv13992332, essv13992324, essv13992340, essv13992330, essv13992383, essv13992380, essv13992379, essv13992362, essv13992317, essv13992363, essv13992382, essv13992333, essv13992310, essv13992385, essv13992347, essv13992410, essv13992358, essv13992408, essv13992394, essv13992377, essv13992386, essv13992360, essv13992364, essv13992355, essv13992407, essv13992375, essv13992352, essv13992338, essv13992369, essv13992387, essv13992329, essv13992404, essv13992341, essv13992321, essv13992335, essv13992398, essv13992322, essv13992325, essv13992372, essv13992414, essv13992312, essv13992349, essv13992376, essv13992400, essv13992314, essv13992359, essv13992339, essv13992311, essv13992389, essv13992319, essv13992354, essv13992313, essv13992356, essv13992323, essv13992328, essv13992368, essv13992315, essv13992351, essv13992413, essv13992373, essv13992353, essv13992348, essv13992402, essv13992346, essv13992396, essv13992401, essv13992381, essv13992370, essv13992403, essv13992384, essv13992393, essv13992318, essv13992391, essv13992392, essv13992350, essv13992405, essv13992345, essv13992342, essv13992326, essv13992361, essv13992343, essv13992399, essv13992337, essv13992406, essv13992371, essv13992366, essv13992390, essv13992327, essv13992316, essv13992395, essv13992409, essv13992331, essv13992320, essv13992412, essv13992336, essv13992334, essv13992397, essv13992378, essv13992374
SamplesNA18998, NA20339, NA19028, NA19700, NA19794, HG02002, HG01624, NA18647, HG00351, NA19734, NA18979, NA18999, NA18641, NA18639, NA20298, HG02277, HG00452, NA19314, HG00097, HG02285, HG00356, NA12812, HG02140, HG02485, HG02087, HG01277, NA19307, NA18567, NA18993, HG00129, NA18574, HG02301, NA18642, HG00355, NA21108, HG00311, NA19038, HG02278, NA19922, NA19923, NA19041, HG02003, NA21109, HG01628, NA18748, HG02082, NA21107, HG02138, NA18640, NA21105, NA21106, NA18645, HG02136, NA18525, HG02090, NA19086, HG01344, NA19984, NA19184, HG02084, NA18939, HG01345, HG02508, HG02497, NA18757, HG00373, HG00350, NA19113, HG02141, NA19001, NA19752, NA19740, HG02081, HG02286, NA19095, HG02484, HG00128, NA19035, NA19308, HG00382, HG02089, NA21117, NA19309, NA19149, NA19735, HG02088, HG02064, NA12873, HG01623, NA19310, HG01620, NA18643, HG00319, NA12874, HG00269, NA19096, HG01105, HG01914, NA19121, NA18957, NA19316, NA21104, NA18740, HG01618, NA18997
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625102
Frequency
Sample Size2504
Observed Gain105
Observed Loss0
Observed Complex0
Frequencyn/a


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