A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587355



Internal ID16028078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30185998..30289834hg38UCSC Ensembl
Innerchr21:31558316..31662152hg19UCSC Ensembl
Innerchr21:30480187..30584023hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38103837
hg19103837
hg18103837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946599
Samples
Known GenesCLDN8, KRTAP24-1, KRTAP25-1, LINC00307
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587355
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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