A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038393



Internal ID18780924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41791376..41895837hg38UCSC Ensembl
Innerchr15:42083574..42188035hg19UCSC Ensembl
Innerchr15:39870866..39975327hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38104462
hg19104462
hg18104462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2582n100
Supporting Variantsnssv3552266
Samples
Known GenesJMJD7, JMJD7-PLA2G4B, MAPKBP1, MIR4310, PLA2G4B, SPTBN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038393
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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