A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685475



Internal ID15075441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2650464..2870706hg38UCSC Ensembl
Innerchr10:2692656..2912898hg19UCSC Ensembl
Innerchr10:2682656..2902898hg18UCSC Ensembl
Innerchr10:2682656..2902898hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38220243
hg19220243
hg18220243
hg17220243
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517630
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685475
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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