A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937909



Internal ID15885179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7571617..8336371hg38UCSC Ensembl
Innerchr20:7552264..8317018hg19UCSC Ensembl
Innerchr20:7500264..8265018hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38764755
hg19764755
hg18764755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585384
Supporting Variants
Samples
Known GenesHAO1, PLCB1, TMX4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv937909
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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