A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586367



Internal ID16373776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58891536..58898939hg38UCSC Ensembl
Innerchr20:57466591..57473994hg19UCSC Ensembl
Innerchr20:56899986..56907389hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg387404
hg197404
hg187404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941811
Samples
Known GenesGNAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586367
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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