A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682405



Internal ID15072371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:50134964..50137139hg38UCSC Ensembl
Innerchr3:50172397..50174572hg19UCSC Ensembl
Innerchr3:50147401..50149576hg18UCSC Ensembl
Innerchr3:50147401..50149576hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382176
hg192176
hg182176
hg172176
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515986
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682405
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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