A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999076



Internal ID18811926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68394343..68615992hg38UCSC Ensembl
Innerchr4:69260061..69481710hg19UCSC Ensembl
Innerchr4:68942656..69164305hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38221650
hg19221650
hg18221650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5243n100
Supporting Variantsnssv3626811
Samples
Known GenesTMPRSS11E, UGT2B17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999076
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