A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586180



Internal ID16373589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:51117002..51144659hg38UCSC Ensembl
Innerchr20:49733539..49761196hg19UCSC Ensembl
Innerchr20:49166946..49194603hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3827658
hg1927658
hg1827658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150958
Samples1780854341_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586180
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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