A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587321



Internal ID16374730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:24752784..24778222hg38UCSC Ensembl
Innerchr21:26125098..26150536hg19UCSC Ensembl
Innerchr21:25046969..25072407hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3825439
hg1925439
hg1825439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946577
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587321
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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