A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938971



Internal ID16232927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24667089..24704804hg38UCSC Ensembl
Innerchr20:24647725..24685440hg19UCSC Ensembl
Innerchr20:24595725..24633440hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3837716
hg1937716
hg1837716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585744
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)nssv938971
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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