A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066010



Internal ID18808541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669231..15709516hg38UCSC Ensembl
Innerchr19:15780041..15820326hg19UCSC Ensembl
Innerchr19:15641041..15681326hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3840286
hg1940286
hg1840286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3446n100
Supporting Variantsnssv3564848, nssv3564850, nssv3564852, nssv3564849, nssv3564851, nssv3564847, nssv3564861, nssv3564856, nssv3564857, nssv3564858, nssv3564853, nssv3564854, nssv3564855, nssv3564860, nssv3564859, nssv3564845, nssv3564846
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)nsv1066010
Frequency
Sample Size29084
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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