A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522837



Internal ID15450130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140035635..140049929hg38UCSC Ensembl
Innerchr8:141045732..141060027hg19UCSC Ensembl
Innerchr8:141114914..141129209hg18UCSC Ensembl
Innerchr8:141114914..141129209hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3814295
hg1914296
hg1814296
hg1714296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698488
Samples
Known GenesTRAPPC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522837
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer