A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946769



Internal ID15894039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37756813..37771724hg38UCSC Ensembl
Innerchr21:39129116..39144027hg19UCSC Ensembl
Innerchr21:38050986..38065897hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3814912
hg1914912
hg1814912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587473
Supporting Variants
Samples
Known GenesKCNJ6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946769
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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