A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587361



Internal ID16374770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30990059..31071890hg38UCSC Ensembl
Innerchr21:32362378..32444209hg19UCSC Ensembl
Innerchr21:31284249..31366080hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3881832
hg1981832
hg1881832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946603
Samples
Known GenesKRTAP19-8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587361
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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