A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938922



Internal ID16232878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24008390..24043622hg38UCSC Ensembl
Innerchr20:23989027..24024259hg19UCSC Ensembl
Innerchr20:23937027..23972259hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3835233
hg1935233
hg1835233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585731
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)nssv938922
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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