A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695786



Internal ID15432438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166799462..166815639hg38UCSC Ensembl
Innerchr3:166517250..166533427hg19UCSC Ensembl
Innerchr3:167999944..168016121hg18UCSC Ensembl
Innerchr3:167999952..168016129hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3816178
hg1916178
hg1816178
hg1716178
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518359
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695786
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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