A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515937



Internal ID15442994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92900376..92965751hg38UCSC Ensembl
Innerchr10:94660133..94725508hg19UCSC Ensembl
Innerchr10:94650113..94715488hg18UCSC Ensembl
Innerchr10:94650113..94715488hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3865376
hg1965376
hg1865376
hg1765376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705699, nssv669234, nssv665380, nssv679213
Samples
Known GenesEXOC6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515937
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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