A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613732



Internal ID16054455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19419530..19594813hg38UCSC Ensembl
Innerchr9:19419528..19594811hg19UCSC Ensembl
Innerchr9:19409528..19584811hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38175284
hg19175284
hg18175284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130785
Samples
Known GenesACER2, SLC24A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613732
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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