A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679213



Internal ID15415865
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 StatusS
Merged Variantsnsv515937
Supporting Variants
Samples
Known GenesEXOC6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679213
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer