A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700559



Internal ID15437211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:26901133..26904717hg38UCSC Ensembl
Innerchr8:26758650..26762234hg19UCSC Ensembl
Innerchr8:26814567..26818151hg18UCSC Ensembl
Innerchr8:26814567..26818151hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg383585
hg193585
hg183585
hg173585
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524598
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700559
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