A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705666



Internal ID15442318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172864812..172873569hg38UCSC Ensembl
Innerchr3:172582602..172591359hg19UCSC Ensembl
Innerchr3:174065296..174074053hg18UCSC Ensembl
Innerchr3:174065304..174074061hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg388758
hg198758
hg188758
hg178758
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528967
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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