A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587337



Internal ID16374746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:26697718..26720212hg38UCSC Ensembl
Innerchr21:28070037..28092531hg19UCSC Ensembl
Innerchr21:26991908..27014402hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3822495
hg1922495
hg1822495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151598
Samples1780854459_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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