A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696508



Internal ID15433160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:26907430..26931691hg38UCSC Ensembl
Innerchr8:26764947..26789208hg19UCSC Ensembl
Innerchr8:26820864..26845125hg18UCSC Ensembl
Innerchr8:26820864..26845125hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3824262
hg1924262
hg1824262
hg1724262
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519039
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696508
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