A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv935238



Internal ID16229194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:641181..642438hg38UCSC Ensembl
Innerchr20:621825..623082hg19UCSC Ensembl
Innerchr20:569825..571082hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381258
hg191258
hg181258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585183
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)nssv935238
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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