A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017694



Internal ID19106911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24912775..25041800hg38UCSC Ensembl
Innerchr7:24952394..25081419hg19UCSC Ensembl
Innerchr7:24918919..25047944hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38129026
hg19129026
hg18129026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752928
Samples
Known GenesOSBPL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017694
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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