A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523900



Internal ID15451193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:39134100..39137263hg38UCSC Ensembl
Innerchr21:40506026..40509189hg19UCSC Ensembl
Innerchr21:39427896..39431059hg18UCSC Ensembl
Innerchr21:39427896..39431059hg17UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg383164
hg193164
hg183164
hg173164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699743
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523900
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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