A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653453



Internal ID15390105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20494784..20521596hg38UCSC Ensembl
Innerchr10:20783713..20810525hg19UCSC Ensembl
Innerchr10:20823719..20850531hg18UCSC Ensembl
Innerchr10:20823719..20850531hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3826813
hg1926813
hg1826813
hg1726813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516763
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653453
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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