A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585933



Internal ID16026656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34654522..34655736hg38UCSC Ensembl
Innerchr20:33242326..33243540hg19UCSC Ensembl
Innerchr20:32705987..32707201hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381215
hg191215
hg181215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939310, nssv939309
Samples
Known GenesPIGU
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585933
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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