A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938967



Internal ID16232923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24431218..24441617hg38UCSC Ensembl
Innerchr20:24411854..24422253hg19UCSC Ensembl
Innerchr20:24359854..24370253hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3810400
hg1910400
hg1810400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585741
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)nssv938967
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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