A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3475227



Internal ID19066389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17262498..17290602hg38UCSC Ensembl
Innerchr1:17588993..17617097hg19UCSC Ensembl
Innerchr1:17461580..17489684hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3828105
hg1928105
hg1828105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007323
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)nssv3475227
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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