A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704785



Internal ID15441437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193860981..193861172hg38UCSC Ensembl
Innerchr3:193578770..193578961hg19UCSC Ensembl
Innerchr3:195061464..195061655hg18UCSC Ensembl
Innerchr3:195061472..195061663hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38192
hg19192
hg18192
hg17192
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528224
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704785
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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