A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705174



Internal ID15441826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46031220..46204989hg38UCSC Ensembl
Innerchr8:46942842..47116611hg19UCSC Ensembl
Innerchr8:47062007..47235776hg18UCSC Ensembl
Innerchr8:47062007..47235776hg17UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38173770
hg19173770
hg18173770
hg17173770
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705174
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