A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003912



Internal ID19093130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68418861..68615992hg38UCSC Ensembl
Innerchr4:69284579..69481710hg19UCSC Ensembl
Innerchr4:68967174..69164305hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38197132
hg19197132
hg18197132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5249n100
Supporting Variantsnssv3626837
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)nsv1003912
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