A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586308



Internal ID16373717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56833797..56851305hg38UCSC Ensembl
Innerchr20:55408853..55426361hg19UCSC Ensembl
Innerchr20:54842260..54859768hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3817509
hg1917509
hg1817509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7617n54
Supporting Variantsnssv941606, nssv941603, nssv941602, nssv1151376, nssv941604, nssv941605
Samples1780862345_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586308
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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