A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587632



Internal ID16028355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42459891..42472765hg38UCSC Ensembl
Innerchr21:43880001..43892875hg19UCSC Ensembl
Innerchr21:42753070..42765944hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3812875
hg1912875
hg1812875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947355
Samples
Known GenesRSPH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587632
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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