A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031119



Internal ID19120340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110355710..110708534hg38UCSC Ensembl
Innerchr8:111367939..111720763hg19UCSC Ensembl
Innerchr8:111437115..111789939hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38352825
hg19352825
hg18352825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757339
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031119
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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