A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035998



Internal ID18778529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41806698..42142056hg38UCSC Ensembl
Innerchr15:42098896..42434254hg19UCSC Ensembl
Innerchr15:39886188..40221546hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38335359
hg19335359
hg18335359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552273
Samples
Known GenesEHD4, JMJD7, JMJD7-PLA2G4B, MAPKBP1, MIR4310, PLA2G4B, PLA2G4D, PLA2G4E, PLA2G4F, SPTBN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035998
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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