A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063989



Internal ID19153208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669231..15683959hg38UCSC Ensembl
Innerchr19:15780041..15794769hg19UCSC Ensembl
Innerchr19:15641041..15655769hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3814729
hg1914729
hg1814729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3448n100
Supporting Variantsnssv3564831, nssv3564833, nssv3564832
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)nsv1063989
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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