A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527146



Internal ID15454439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35644365..35684975hg38UCSC Ensembl
Innerchr21:37016663..37057273hg19UCSC Ensembl
Innerchr21:35938533..35979143hg18UCSC Ensembl
Innerchr21:35938533..35979143hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3840611
hg1940611
hg1840611
hg1740611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703535
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527146
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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