A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065116



Internal ID19154335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15688466..15713261hg38UCSC Ensembl
Innerchr19:15799276..15824071hg19UCSC Ensembl
Innerchr19:15660276..15685071hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3824796
hg1924796
hg1824796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3453n100
Supporting Variantsnssv3569777
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)nsv1065116
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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