A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064340



Internal ID18806871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669231..15680854hg38UCSC Ensembl
Innerchr19:15780041..15791664hg19UCSC Ensembl
Innerchr19:15641041..15652664hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3811624
hg1911624
hg1811624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3450n100
Supporting Variantsnssv3564829, nssv3564830
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)nsv1064340
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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