A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939319



Internal ID15886589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34654834..34655671hg38UCSC Ensembl
Innerchr20:33242638..33243475hg19UCSC Ensembl
Innerchr20:32706299..32707136hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38838
hg19838
hg18838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585937
Supporting Variants
Samples
Known GenesPIGU
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939319
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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