A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528466



Internal ID15455759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:167545714..167591341hg38UCSC Ensembl
Innerchr2:168402224..168447851hg19UCSC Ensembl
Innerchr2:168110470..168156097hg18UCSC Ensembl
Innerchr2:168227731..168273358hg17UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3845628
hg1945628
hg1845628
hg1745628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705068
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528466
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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