A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585667



Internal ID16373076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18209123..18210515hg38UCSC Ensembl
Innerchr20:18189767..18191159hg19UCSC Ensembl
Innerchr20:18137767..18139159hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381393
hg191393
hg181393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938596, nssv938597, nssv938595
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585667
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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