A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587720



Internal ID16028443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43812441..43844039hg38UCSC Ensembl
Innerchr21:45232322..45263920hg19UCSC Ensembl
Innerchr21:44056750..44088348hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3831599
hg1931599
hg1831599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948046
Samples
Known GenesLOC284837
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587720
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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