A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520827



Internal ID15101434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:34365859..34369557hg38UCSC Ensembl
Innerchr21:35738158..35741856hg19UCSC Ensembl
Innerchr21:34660028..34663726hg18UCSC Ensembl
Innerchr21:34660028..34663726hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383699
hg193699
hg183699
hg173699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680113, nssv676036, nssv680587
Samples
Known GenesKCNE2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520827
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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