A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637431



Internal ID7024223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99723812..99724352hg38UCSC Ensembl
Innerchr15:99723812..99724352hg38UCSC Ensembl
Outerchr15:99723444..99724653hg38UCSC Ensembl
chr15:100264017..100264557hg19UCSC Ensembl
Innerchr15:100264017..100264557hg19UCSC Ensembl
Outerchr15:100263649..100264858hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15345220, essv15345293, essv15345274, essv15345214, essv15345308, essv15345304, essv15345272, essv15345255, essv15345203, essv15345242, essv15345278, essv15345286, essv15345307, essv15345208, essv15345222, essv15345265, essv15345277, essv15345193, essv15345313, essv15345317, essv15345238, essv15345275, essv15345269, essv15345302, essv15345247, essv15345253, essv15345273, essv15345298, essv15345291, essv15345292, essv15345266, essv15345270, essv15345207, essv15345251, essv15345234, essv15345289, essv15345288, essv15345235, essv15345227, essv15345294, essv15345271, essv15345233, essv15345295, essv15345209, essv15345230, essv15345239, essv15345216, essv15345296, essv15345228, essv15345200, essv15345282, essv15345254, essv15345202, essv15345311, essv15345315, essv15345264, essv15345256, essv15345206, essv15345300, essv15345260, essv15345301, essv15345312, essv15345236, essv15345243, essv15345205, essv15345226, essv15345191, essv15345250, essv15345263, essv15345244, essv15345223, essv15345309, essv15345241, essv15345262, essv15345306, essv15345192, essv15345297, essv15345218, essv15345198, essv15345299, essv15345261, essv15345310, essv15345232, essv15345225, essv15345201, essv15345279, essv15345290, essv15345229, essv15345305, essv15345281, essv15345213, essv15345314, essv15345276, essv15345194, essv15345199, essv15345287, essv15345268, essv15345196, essv15345237, essv15345211, essv15345221, essv15345285, essv15345215, essv15345248, essv15345246, essv15345303, essv15345283, essv15345217, essv15345280, essv15345257, essv15345316, essv15345224, essv15345258, essv15345284, essv15345318, essv15345204, essv15345240, essv15345195, essv15345210, essv15345212, essv15345219, essv15345231, essv15345197, essv15345267, essv15345259, essv15345245, essv15345249, essv15345252
SamplesNA18502, NA20339, HG03559, NA19222, HG02944, HG02496, NA19909, NA19204, HG03057, HG02337, NA18881, HG02419, NA19020, HG03521, HG03280, NA20294, HG03455, NA18870, HG03372, NA19107, HG02811, HG03135, HG03499, HG02840, NA19916, HG03370, NA19138, HG03224, HG03040, NA20291, HG01110, HG02281, NA19922, HG03209, HG02143, HG03520, NA19917, HG03212, HG01440, HG03352, HG02571, NA20412, NA19189, NA19239, NA18864, HG03267, HG01709, HG02623, NA19025, HG03055, NA20127, HG03394, NA19451, HG03270, HG03169, HG03343, HG03120, NA19247, NA19707, NA19462, NA19984, HG03547, HG03291, HG02511, HG02108, HG02322, NA18516, NA19982, HG03428, HG02953, NA18910, NA18871, HG02537, HG01047, HG03472, NA19449, HG03136, HG03397, HG01241, HG02884, HG03024, NA19452, NA19318, HG02332, HG01956, HG01107, HG01075, HG02484, HG02255, HG02613, HG02455, HG02330, HG02282, NA19147, NA20276, HG01894, NA19435, HG03458, HG02923, NA19380, HG03127, NA19439, NA19428, NA19360, HG03557, NA19323, NA19143, HG03432, HG03039, NA19248, NA19472, NA19351, HG03313, NA19468, HG02938, NA19093, HG03060, HG03351, NA18873, HG02051, HG01883, HG02861, NA18505, NA18488, NA18522, HG00554, NA19214, HG03166
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637431
Frequency
Sample Size2504
Observed Gain0
Observed Loss128
Observed Complex0
Frequencyn/a


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