A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065592



Internal ID19154811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15613287..15638182hg38UCSC Ensembl
Innerchr19:15724098..15748992hg19UCSC Ensembl
Innerchr19:15585098..15609992hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3824896
hg1924895
hg1824895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3444n100
Supporting Variantsnssv3564800
Samples
Known GenesCYP4F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065592
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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