A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661579



Internal ID9927684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4395550..4399121hg38UCSC Ensembl
Outerchr10:4395393..4399274hg38UCSC Ensembl
Innerchr10:4437742..4441313hg19UCSC Ensembl
Outerchr10:4437585..4441466hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383882
hg193882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5842912, essv5950203, essv5720126, essv5475126, essv6212532, essv6527189, essv6112144, essv6043207, essv5933065, essv6466325, essv5451333, essv6167619, essv6202574, essv6232393, essv6204431, essv6117606, essv5508372, essv5808340, essv6198026, essv6350599, essv5769565, essv5412347, essv6343470, essv6030663, essv5613386, essv6425792, essv5546152, essv6531952, essv6237823, essv6353718, essv5850517, essv5676154, essv5825528, essv5457607, essv6105350, essv6281956, essv6198279, essv6027121, essv5849825, essv6079243, essv6308168, essv6373234
SamplesNA19700, HG01462, NA19399, NA19350, NA19359, NA19092, NA19819, NA19377, NA19107, NA19171, NA19198, NA19313, NA19904, NA19917, NA19371, NA19235, NA19385, NA19471, NA19901, NA18520, NA18908, NA19908, NA19437, NA19347, NA18910, NA19338, NA18523, NA19440, NA19390, NA18909, NA19435, NA19248, NA19472, NA19102, NA19711, NA19900, NA18505, NA19129, NA18488, NA19316, NA18487, NA19431
Known GenesLINC00703
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661579
Frequency
Sample Size1151
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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