A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv948410



Internal ID15895680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44977045..45028338hg38UCSC Ensembl
Innerchr21:46396960..46448253hg19UCSC Ensembl
Innerchr21:45221388..45272681hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3851294
hg1951294
hg1851294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587818
Supporting Variants
Samples
Known GenesLINC00162, LINC00163
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv948410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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