A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694447



Internal ID15431099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139735851..139739776hg38UCSC Ensembl
Innerchr8:140748094..140752019hg19UCSC Ensembl
Innerchr8:140817276..140821201hg18UCSC Ensembl
Innerchr8:140817276..140821201hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383926
hg193926
hg183926
hg173926
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521446
Supporting Variants
Samples
Known GenesTRAPPC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694447
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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