A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615194



Internal ID16402603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111715190..111795195hg38UCSC Ensembl
Innerchr9:114477470..114557475hg19UCSC Ensembl
Innerchr9:113517291..113597296hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3880006
hg1980006
hg1880006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141241
Samples
Known GenesC9orf84
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615194
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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