A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697238



Internal ID15087204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13742515..13761728hg38UCSC Ensembl
Innerchr8:13600024..13619237hg19UCSC Ensembl
Innerchr8:13644395..13663608hg18UCSC Ensembl
Innerchr8:13644395..13663608hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3819214
hg1919214
hg1819214
hg1719214
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697238
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