A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999762



Internal ID19159298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165541222..165578732hg38UCSC Ensembl
Innerchr3:165259010..165296520hg19UCSC Ensembl
Innerchr3:166741704..166779214hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3837511
hg1937511
hg1837511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4973n100
Supporting Variantsnssv3612552
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999762
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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