A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653236



Internal ID15389888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69777409..69779825hg38UCSC Ensembl
Innerchr10:71537165..71539581hg19UCSC Ensembl
Innerchr10:71207171..71209587hg18UCSC Ensembl
Innerchr10:71207171..71209587hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382417
hg192417
hg182417
hg172417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517781
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653236
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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