A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058473



Internal ID19147692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15670535..15722633hg38UCSC Ensembl
Innerchr19:15781345..15833443hg19UCSC Ensembl
Innerchr19:15642345..15694443hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3852099
hg1952099
hg1852099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3447n100
Supporting Variantsnssv3568632
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)nsv1058473
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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