A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637334



Internal ID7024127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95500134..95503006hg38UCSC Ensembl
Innerchr15:95500634..95502506hg38UCSC Ensembl
Outerchr15:95499134..95504006hg38UCSC Ensembl
chr15:96043363..96046235hg19UCSC Ensembl
Innerchr15:96043863..96045735hg19UCSC Ensembl
Outerchr15:96042363..96047235hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382873
hg192873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15326219, essv15326233, essv15326370, essv15326235, essv15326375, essv15326265, essv15326254, essv15326244, essv15326234, essv15326364, essv15326290, essv15326284, essv15326220, essv15326215, essv15326363, essv15326337, essv15326298, essv15326309, essv15326310, essv15326269, essv15326217, essv15326222, essv15326327, essv15326273, essv15326237, essv15326247, essv15326242, essv15326280, essv15326316, essv15326259, essv15326276, essv15326251, essv15326231, essv15326320, essv15326377, essv15326323, essv15326367, essv15326357, essv15326227, essv15326322, essv15326325, essv15326268, essv15326365, essv15326335, essv15326252, essv15326317, essv15326305, essv15326307, essv15326294, essv15326285, essv15326279, essv15326271, essv15326355, essv15326329, essv15326303, essv15326306, essv15326354, essv15326349, essv15326261, essv15326347, essv15326361, essv15326359, essv15326304, essv15326331, essv15326258, essv15326288, essv15326308, essv15326326, essv15326226, essv15326358, essv15326278, essv15326374, essv15326366, essv15326333, essv15326262, essv15326346, essv15326313, essv15326241, essv15326334, essv15326299, essv15326272, essv15326300, essv15326292, essv15326236, essv15326344, essv15326214, essv15326246, essv15326243, essv15326274, essv15326336, essv15326330, essv15326224, essv15326248, essv15326376, essv15326255, essv15326343, essv15326350, essv15326270, essv15326223, essv15326341, essv15326312, essv15326283, essv15326267, essv15326213, essv15326239, essv15326324, essv15326257, essv15326362, essv15326372, essv15326250, essv15326266, essv15326338, essv15326291, essv15326314, essv15326295, essv15326339, essv15326229, essv15326342, essv15326287, essv15326296, essv15326221, essv15326260, essv15326328, essv15326249, essv15326371, essv15326351, essv15326319, essv15326373, essv15326253, essv15326297, essv15326263, essv15326240, essv15326225, essv15326356, essv15326230, essv15326282, essv15326348, essv15326352, essv15326345, essv15326315, essv15326264, essv15326360, essv15326340, essv15326228, essv15326218, essv15326332, essv15326256, essv15326318, essv15326216, essv15326277, essv15326301, essv15326286, essv15326238, essv15326311, essv15326321, essv15326275, essv15326302, essv15326245, essv15326368, essv15326293, essv15326369, essv15326281, essv15326353, essv15326289, essv15326232
SamplesHG02614, HG01173, NA19700, HG02610, NA18924, HG02583, HG03163, HG04060, HG00100, NA19704, NA12843, HG01326, HG03300, HG01389, NA20752, HG03115, HG02870, HG02804, NA20298, NA19819, HG01486, NA19393, NA18878, HG03100, NA12058, HG03297, HG03139, HG03172, HG02888, HG02589, HG03069, NA20359, HG02769, HG03095, HG03074, NA19171, HG02621, NA19319, HG02811, NA19448, HG03091, HG02325, NA19198, HG02756, HG03370, HG01459, HG03874, HG02645, HG03479, HG03224, HG03040, HG03079, HG02281, HG03209, HG02562, HG02315, NA18874, HG03268, HG03212, HG02461, NA19372, NA19235, HG01284, HG02588, NA19036, NA19026, NA20412, NA19239, HG01058, NA12828, HG03058, HG02623, HG03583, HG01275, NA20515, HG03169, HG02716, HG03343, HG02442, HG02977, HG03054, HG01435, HG04039, HG02334, HG02582, NA20885, HG02678, HG03291, NA19391, HG02108, HG02322, NA18915, HG02144, NA12718, HG01880, HG03027, HG02537, HG01047, HG02429, HG01414, HG03476, HG02817, HG02577, HG02445, NA18856, HG01241, HG02881, NA20282, NA19257, NA19452, HG02332, NA19095, NA20296, NA20821, NA19308, HG02613, HG03028, HG02282, NA19256, NA18517, HG03437, HG02308, HG02220, HG02983, HG01894, HG02837, NA20520, NA19439, NA19324, HG02580, NA12874, HG03557, HG01342, HG02558, NA19376, HG03565, NA20348, HG02971, NA19472, NA19223, HG01302, HG01055, HG03063, HG03060, HG00174, HG02239, HG01914, HG03445, HG02855, NA19146, HG01125, HG03072, HG02805, NA18511, HG02808, HG02629, HG00180, HG01786, NA19429, HG01437, HG01061, HG03166, NA19431, HG03265, HG02760
Known GenesLINC00924
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637334
Frequency
Sample Size2504
Observed Gain0
Observed Loss165
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer