A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176140



Internal ID15529169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113482702..113600458hg38UCSC Ensembl
Innerchr9:116244982..116362738hg19UCSC Ensembl
Innerchr9:115284803..115402559hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38117757
hg19117757
hg18117757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615215
Supporting Variants
SamplesHGDP00746
Known GenesRGS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176140
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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