A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016883



Internal ID18759418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62198182..62258795hg38UCSC Ensembl
Innerchr8:63110741..63171354hg19UCSC Ensembl
Innerchr8:63273295..63333908hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3860614
hg1960614
hg1860614
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689473
Samples
Known GenesNKAIN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016883
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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