A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3463732



Internal ID19060317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17262498..17296402hg38UCSC Ensembl
Innerchr1:17588993..17622897hg19UCSC Ensembl
Innerchr1:17461580..17495484hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3833905
hg1933905
hg1833905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997473
Supporting Variants
Samples
Known GenesPADI3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3463732
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