A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528517



Internal ID15109124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41865317..41865721hg38UCSC Ensembl
Innerchr21:43285426..43285830hg19UCSC Ensembl
Innerchr21:42158495..42158899hg18UCSC Ensembl
Innerchr21:42158495..42158899hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38405
hg19405
hg18405
hg17405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705126
Samples
Known GenesPRDM15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528517
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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