A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665363



Internal ID15402015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145908581..145942575hg38UCSC Ensembl
Innerchr3:145626368..145660362hg19UCSC Ensembl
Innerchr3:147109058..147143052hg18UCSC Ensembl
Innerchr3:147109066..147143060hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3833995
hg1933995
hg1833995
hg1733995
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517206
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665363
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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