A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686236



Internal ID15076202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13758356..13773949hg38UCSC Ensembl
Innerchr8:13615865..13631458hg19UCSC Ensembl
Innerchr8:13660236..13675829hg18UCSC Ensembl
Innerchr8:13660236..13675829hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3815594
hg1915594
hg1815594
hg1715594
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)nssv686236
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