A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656962



Internal ID15046928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5604140..5673438hg38UCSC Ensembl
Innerchr10:5646103..5715401hg19UCSC Ensembl
Innerchr10:5686109..5755407hg18UCSC Ensembl
Innerchr10:5686109..5755407hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3869299
hg1969299
hg1869299
hg1769299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519582
Supporting Variants
Samples
Known GenesASB13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656962
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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