A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585687



Internal ID16373096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19924112..19925071hg38UCSC Ensembl
Innerchr20:19904756..19905715hg19UCSC Ensembl
Innerchr20:19852756..19853715hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38960
hg19960
hg18960
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938770, nssv938769
Samples
Known GenesRIN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585687
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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