A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676705



Internal ID15413357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:66511762..66519871hg38UCSC Ensembl
Innerchr8:67423997..67432106hg19UCSC Ensembl
Innerchr8:67586551..67594660hg18UCSC Ensembl
Innerchr8:67586551..67594660hg17UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg388110
hg198110
hg188110
hg178110
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)nssv676705
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