A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3626881



Internal ID18925162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68422408..68592208hg38UCSC Ensembl
Innerchr4:69288126..69457926hg19UCSC Ensembl
Innerchr4:68970721..69140521hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38169801
hg19169801
hg18169801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012499
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)nssv3626881
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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