A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036153



Internal ID18778684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41806698..41895837hg38UCSC Ensembl
Innerchr15:42098896..42188035hg19UCSC Ensembl
Innerchr15:39886188..39975327hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3889140
hg1989140
hg1889140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2582n100
Supporting Variantsnssv3552272, nssv3552271
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)nsv1036153
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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