A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013420



Internal ID19102638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68450721..68674295hg38UCSC Ensembl
Innerchr4:69316439..69540013hg19UCSC Ensembl
Innerchr4:68999034..69222608hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38223575
hg19223575
hg18223575
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5251n100
Supporting Variantsnssv3627056, nssv3627058, nssv3740244, nssv3627057
Samples
Known GenesTMPRSS11E, UGT2B15, UGT2B17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013420
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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