A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564799



Internal ID18863080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15609874..15638182hg38UCSC Ensembl
Innerchr19:15720685..15748992hg19UCSC Ensembl
Innerchr19:15581685..15609992hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3828309
hg1928308
hg1828308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059028
Supporting Variants
Samples
Known GenesCYP4F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564799
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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