A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564796



Internal ID18863077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15542560..15644632hg38UCSC Ensembl
Innerchr19:15653371..15755442hg19UCSC Ensembl
Innerchr19:15514371..15616442hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38102073
hg19102072
hg18102072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065872
Supporting Variants
Samples
Known GenesCYP4F22, CYP4F3, CYP4F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564796
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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