A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610693



Internal ID6997610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125607005..125609097hg38UCSC Ensembl
Innerchr6:125607021..125609082hg38UCSC Ensembl
Outerchr6:125606990..125609113hg38UCSC Ensembl
chr6:125928151..125930243hg19UCSC Ensembl
Innerchr6:125928167..125930228hg19UCSC Ensembl
Outerchr6:125928136..125930259hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12537295, essv12537238, essv12537285, essv12537282, essv12537269, essv12537234, essv12537273, essv12537225, essv12537242, essv12537296, essv12537264, essv12537274, essv12537268, essv12537292, essv12537239, essv12537290, essv12537279, essv12537210, essv12537245, essv12537259, essv12537301, essv12537244, essv12537216, essv12537248, essv12537288, essv12537275, essv12537214, essv12537271, essv12537277, essv12537236, essv12537299, essv12537246, essv12537291, essv12537223, essv12537280, essv12537286, essv12537254, essv12537289, essv12537219, essv12537272, essv12537232, essv12537212, essv12537228, essv12537249, essv12537266, essv12537278, essv12537283, essv12537297, essv12537240, essv12537258, essv12537305, essv12537211, essv12537300, essv12537306, essv12537243, essv12537294, essv12537251, essv12537250, essv12537217, essv12537213, essv12537222, essv12537253, essv12537257, essv12537270, essv12537229, essv12537261, essv12537241, essv12537256, essv12537231, essv12537303, essv12537230, essv12537226, essv12537298, essv12537302, essv12537284, essv12537252, essv12537215, essv12537287, essv12537218, essv12537227, essv12537304, essv12537262, essv12537224, essv12537281, essv12537247, essv12537265, essv12537260, essv12537220, essv12537235, essv12537255, essv12537263, essv12537267, essv12537237, essv12537276, essv12537233, essv12537221, essv12537293
SamplesHG02574, NA19701, HG03559, NA19222, HG02944, HG02496, HG01965, NA18508, HG01885, HG01359, HG03175, HG03057, HG03300, NA18877, HG02891, HG02804, HG03298, HG02476, HG03455, NA18878, HG02624, HG03295, NA19920, HG02769, HG03199, NA19374, HG03086, HG01110, HG02505, HG02703, HG03189, NA18868, NA20340, NA19235, HG02571, HG03267, HG03073, HG02623, HG03169, HG02009, HG02439, HG03547, HG01879, HG02322, NA19982, HG02953, HG02887, HG03081, HG03027, HG02878, HG02537, HG01447, HG03472, HG02429, HG03446, HG03571, NA19338, HG03391, HG02666, HG02332, NA19095, HG03109, HG02568, HG02675, HG01896, NA19436, NA19206, HG02667, HG03461, NA19256, HG02983, HG02721, HG03117, NA19144, HG02611, HG03433, HG02317, HG03557, HG03112, HG03442, HG03097, HG01556, HG03313, HG03279, HG02938, HG02107, HG03063, HG03060, NA19185, HG03538, HG02052, HG02051, HG01914, HG01883, HG03072, HG01695, HG02760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610693
Frequency
Sample Size2504
Observed Gain0
Observed Loss97
Observed Complex0
Frequencyn/a


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