A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038933



Internal ID18781464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41846258..42016889hg38UCSC Ensembl
Innerchr15:42138456..42309087hg19UCSC Ensembl
Innerchr15:39925748..40096379hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38170632
hg19170632
hg18170632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716702
Samples
Known GenesEHD4, JMJD7-PLA2G4B, MIR4310, PLA2G4B, PLA2G4E, SPTBN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038933
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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