A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585181



Internal ID16372590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:611050..630017hg38UCSC Ensembl
Innerchr20:591694..610661hg19UCSC Ensembl
Innerchr20:539694..558661hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3818968
hg1918968
hg1818968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150944
Samples1780862306_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585181
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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