A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587085



Internal ID16027808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17814297..17886994hg38UCSC Ensembl
Innerchr21:19186614..19259311hg19UCSC Ensembl
Innerchr21:18108485..18181182hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3872698
hg1972698
hg1872698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7768n54
Supporting Variantsnssv945520
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)nsv587085
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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