A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008013



Internal ID18750544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152644272..152889874hg38UCSC Ensembl
Innerchr3:152362061..152607663hg19UCSC Ensembl
Innerchr3:153844751..154090353hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38245603
hg19245603
hg18245603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741542
Samples
Known GenesP2RY1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008013
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