A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528967



Internal ID15456260
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705666
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528967
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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