A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016444



Internal ID19105663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:685389..852451hg38UCSC Ensembl
Innerchr5:685504..852566hg19UCSC Ensembl
Innerchr5:738504..905566hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38167063
hg19167063
hg18167063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5525n100
Supporting Variantsnssv3633313
Samples
Known GenesTPPP, ZDHHC11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016444
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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