A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670085



Internal ID15406737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:66511762..66515557hg38UCSC Ensembl
Innerchr8:67423997..67427792hg19UCSC Ensembl
Innerchr8:67586551..67590346hg18UCSC Ensembl
Innerchr8:67586551..67590346hg17UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg383796
hg193796
hg183796
hg173796
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516599
Supporting Variants
Samples
Known GenesC8orf46
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670085
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