A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065577



Internal ID18808108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669691..15714929hg38UCSC Ensembl
Innerchr19:15780501..15825739hg19UCSC Ensembl
Innerchr19:15641501..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3845239
hg1945239
hg1845239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3446n100
Supporting Variantsnssv3568617, nssv3568616
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)nsv1065577
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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