A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3626879



Internal ID18578474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68422408..68564420hg38UCSC Ensembl
Innerchr4:69288126..69430138hg19UCSC Ensembl
Innerchr4:68970721..69112733hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38142013
hg19142013
hg18142013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999186
Supporting Variants
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)nssv3626879
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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