A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055298



Internal ID19144517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15613287..15642613hg38UCSC Ensembl
Innerchr19:15724098..15753423hg19UCSC Ensembl
Innerchr19:15585098..15614423hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3829327
hg1929326
hg1829326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3445n100
Supporting Variantsnssv3564802, nssv3564801
Samples
Known GenesCYP4F3, CYP4F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055298
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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