A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176112



Internal ID15875410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109070362..109087452hg38UCSC Ensembl
Innerchr9:111832642..111849732hg19UCSC Ensembl
Innerchr9:110872463..110889553hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3817091
hg1917091
hg1817091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615148
Supporting Variants
SamplesHGDP00681
Known GenesTMEM245
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176112
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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