A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145318



Internal ID15651818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131487491..131566642hg38UCSC Ensembl
Innerchr9:134362878..134442029hg19UCSC Ensembl
Innerchr9:133352699..133431850hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3879152
hg1979152
hg1879152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615563
Supporting Variants
Samples
Known GenesPOMT1, PRRC2B, SNORD62A, SNORD62B, UCK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145318
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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