A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587084



Internal ID16027807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17814297..17876803hg38UCSC Ensembl
Innerchr21:19186614..19249120hg19UCSC Ensembl
Innerchr21:18108485..18170991hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3862507
hg1962507
hg1862507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7768n54
Supporting Variantsnssv945519
Samples
Known GenesC21orf91, CHODL-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587084
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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