A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946770



Internal ID15894040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37783651..37838703hg38UCSC Ensembl
Innerchr21:39155954..39211005hg19UCSC Ensembl
Innerchr21:38077824..38132875hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3855053
hg1955052
hg1855052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587474
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)nssv946770
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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