A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613196



Internal ID16053919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5345673..5514372hg38UCSC Ensembl
Innerchr9:5345673..5514372hg19UCSC Ensembl
Innerchr9:5335673..5504372hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38168700
hg19168700
hg18168700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156217
Samples1798860570_A
Known GenesCD274, PDCD1LG2, PLGRKT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613196
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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