A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058398



Internal ID18800929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15679275..15714929hg38UCSC Ensembl
Innerchr19:15790085..15825739hg19UCSC Ensembl
Innerchr19:15651085..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3835655
hg1935655
hg1835655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3452n100
Supporting Variantsnssv3568648, nssv3568646, nssv3568647
Samples
Known GenesCYP4F12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058398
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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