A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705126



Internal ID15095092
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528517
Supporting Variants
Samples
Known GenesPRDM15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705126
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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