A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585942



Internal ID16026665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34655736..34655852hg38UCSC Ensembl
Innerchr20:33243540..33243656hg19UCSC Ensembl
Innerchr20:32707201..32707317hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38117
hg19117
hg18117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939328, nssv939327, nssv939325, nssv939326, nssv939329
Samples
Known GenesPIGU
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585942
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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