A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141288



Internal ID15994474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116980695..117151329hg38UCSC Ensembl
Innerchr9:119742974..119913608hg19UCSC Ensembl
Innerchr9:118782795..118953429hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38170635
hg19170635
hg18170635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615261
Supporting Variants
Samples
Known GenesASTN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141288
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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