A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1124239



Internal ID15977425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139737929..139840395hg38UCSC Ensembl
Innerchr8:140750172..140852638hg19UCSC Ensembl
Innerchr8:140819354..140921820hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38102467
hg19102467
hg18102467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612545
Supporting Variants
Samples
Known GenesTRAPPC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1124239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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