A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141277



Internal ID15994463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114330749..114331675hg38UCSC Ensembl
Innerchr9:117093029..117093955hg19UCSC Ensembl
Innerchr9:116132850..116133776hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38927
hg19927
hg18927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615247
Supporting Variants
Samples
Known GenesORM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141277
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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