A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585934



Internal ID16026657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34654522..34655852hg38UCSC Ensembl
Innerchr20:33242326..33243656hg19UCSC Ensembl
Innerchr20:32705987..32707317hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381331
hg191331
hg181331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7561n54
Supporting Variantsnssv939314, nssv939311, nssv939313, nssv939312
Samples
Known GenesPIGU
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585934
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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