A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585644



Internal ID16373053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15786082..15826796hg38UCSC Ensembl
Innerchr20:15766727..15807441hg19UCSC Ensembl
Innerchr20:15714727..15755441hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3840715
hg1940715
hg1840715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7505n54
Supporting Variantsnssv938571
Samples
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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