A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587571



Internal ID16028294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41871888..41891876hg38UCSC Ensembl
Innerchr21:43291997..43311985hg19UCSC Ensembl
Innerchr21:42165066..42185054hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3819989
hg1919989
hg1819989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7851n54
Supporting Variantsnssv947150
Samples
Known GenesC2CD2, PRDM15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587571
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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