A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045142



Internal ID18787673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41292846..41446116hg38UCSC Ensembl
Innerchr15:41585044..41738314hg19UCSC Ensembl
Innerchr15:39372336..39525606hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38153271
hg19153271
hg18153271
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2580n100
Supporting Variantsnssv3552256
Samples
Known GenesNDUFAF1, NUSAP1, OIP5, OIP5-AS1, RTF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045142
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer