A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615259



Internal ID16402668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116849551..117075436hg38UCSC Ensembl
Innerchr9:119611830..119837715hg19UCSC Ensembl
Innerchr9:118651651..118877536hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38225886
hg19225886
hg18225886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141286
Samples
Known GenesASTN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615259
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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