A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697914



Internal ID15087880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3052993..3053089hg38UCSC Ensembl
Innerchr10:3095185..3095281hg19UCSC Ensembl
Innerchr10:3085185..3085281hg18UCSC Ensembl
Innerchr10:3085185..3085281hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3897
hg1997
hg1897
hg1797
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)nssv697914
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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