A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586187



Internal ID16373596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:52035854..52040510hg38UCSC Ensembl
Innerchr20:50652393..50657049hg19UCSC Ensembl
Innerchr20:50085800..50090456hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384657
hg194657
hg184657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940998, nssv940996, nssv940997
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586187
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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