A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521572



Internal ID15102179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41286691..41318043hg38UCSC Ensembl
Innerchr3:41328182..41359534hg19UCSC Ensembl
Innerchr3:41303186..41334538hg18UCSC Ensembl
Innerchr3:41303186..41334538hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3831353
hg1931353
hg1831353
hg1731353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698188
Samples
Known GenesULK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521572
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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