A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662701



Internal ID15399353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62955573..62956783hg38UCSC Ensembl
Innerchr3:62941248..62942458hg19UCSC Ensembl
Innerchr3:62916288..62917498hg18UCSC Ensembl
Innerchr3:62916288..62917498hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381211
hg191211
hg181211
hg171211
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520303
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662701
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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