A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946576



Internal ID16240532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:24340506..24408437hg38UCSC Ensembl
Innerchr21:25712819..25780751hg19UCSC Ensembl
Innerchr21:24634690..24702622hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3867932
hg1967933
hg1867933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587320
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946576
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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