A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624922



Internal ID6665084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129617844..129618789hg38UCSC Ensembl
Innerchr10:129617844..129618789hg38UCSC Ensembl
Outerchr10:129617592..129619074hg38UCSC Ensembl
chr10:131416108..131417053hg19UCSC Ensembl
Innerchr10:131416108..131417053hg19UCSC Ensembl
Outerchr10:131415856..131417338hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13973297, essv13973290, essv13973304, essv13973314, essv13973293, essv13973299, essv13973310, essv13973309, essv13973295, essv13973292, essv13973307, essv13973313, essv13973306, essv13973294, essv13973289, essv13973301, essv13973288, essv13973315, essv13973312, essv13973305, essv13973308, essv13973311, essv13973303, essv13973296, essv13973291, essv13973300, essv13973302, essv13973298
SamplesHG01864, HG00309, NA18952, HG00369, HG02060, HG00632, HG01845, HG02139, NA18969, HG00581, HG00404, HG00319, HG00353, HG00556, HG00308, HG00180, NA18609, HG00268, HG00282, HG02069, NA18619, HG00378, HG00530, HG00656, HG00275, HG02188, HG00336, HG00476
Known GenesMGMT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624922
Frequency
Sample Size2504
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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