A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661637



Internal ID15398289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75333283..75408707hg38UCSC Ensembl
Innerchr3:75382434..75457858hg19UCSC Ensembl
Innerchr3:75465124..75540548hg18UCSC Ensembl
Innerchr3:75465124..75540548hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3875425
hg1975425
hg1875425
hg1775425
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517173
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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