A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587573



Internal ID16028296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41873262..41897914hg38UCSC Ensembl
Innerchr21:43293371..43318023hg19UCSC Ensembl
Innerchr21:42166440..42191092hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3824653
hg1924653
hg1824653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7851n54
Supporting Variantsnssv947152
Samples
Known GenesC2CD2, PRDM15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587573
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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