A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515865



Internal ID15442922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11436705..11442946hg38UCSC Ensembl
Innerchr10:11478704..11484945hg19UCSC Ensembl
Innerchr10:11518710..11524951hg18UCSC Ensembl
Innerchr10:11518710..11524951hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386242
hg196242
hg186242
hg176242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656690, nssv657607, nssv655351, nssv675718, nssv669232, nssv685084, nssv671366, nssv693050, nssv691348, nssv661592, nssv663719, nssv669526, nssv658588, nssv700865, nssv665076, nssv692700, nssv668091, nssv679038, nssv666811, nssv683682, nssv661131, nssv659913, nssv656942, nssv682950
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515865
Frequency
Sample Size2026
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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