A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055310



Internal ID18797841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15681655..15709225hg38UCSC Ensembl
Innerchr19:15792465..15820035hg19UCSC Ensembl
Innerchr19:15653465..15681035hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3827571
hg1927571
hg1827571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3452n100
Supporting Variantsnssv3568649
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)nsv1055310
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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