A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518058



Internal ID15445351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139875396..139902386hg38UCSC Ensembl
Innerchr8:140887640..140914630hg19UCSC Ensembl
Innerchr8:140956822..140983812hg18UCSC Ensembl
Innerchr8:140956822..140983812hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3826991
hg1926991
hg1826991
hg1726991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695469
Samples
Known GenesTRAPPC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518058
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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