A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1109990



Internal ID15963176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:34792032..34852600hg38UCSC Ensembl
Innerchr8:34649550..34710118hg19UCSC Ensembl
Innerchr8:34769092..34829660hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3860569
hg1960569
hg1860569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610933
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1109990
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer