A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661346



Internal ID15397998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47067933..47932297hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17864365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516485
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661346
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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