A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680610



Internal ID15417262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20494784..20533677hg38UCSC Ensembl
Innerchr10:20783713..20822606hg19UCSC Ensembl
Innerchr10:20823719..20862612hg18UCSC Ensembl
Innerchr10:20823719..20862612hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3838894
hg1938894
hg1838894
hg1738894
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)nssv680610
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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