A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660008



Internal ID15396660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94622533..94647861hg38UCSC Ensembl
Innerchr1:95088089..95113417hg19UCSC Ensembl
Innerchr1:94860677..94886005hg18UCSC Ensembl
Innerchr1:94800110..94825438hg17UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3825329
hg1925329
hg1825329
hg1725329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519997
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660008
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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