A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586365



Internal ID16373774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58890621..58893423hg38UCSC Ensembl
Innerchr20:57465676..57468478hg19UCSC Ensembl
Innerchr20:56899071..56901873hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg382803
hg192803
hg182803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7626n54
Supporting Variantsnssv941808, nssv941809, nssv941807
Samples
Known GenesGNAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586365
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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