A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676036



Internal ID15066002
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520827
Supporting Variants
Samples
Known GenesKCNE2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676036
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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