A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057902



Internal ID18800433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669231..15713261hg38UCSC Ensembl
Innerchr19:15780041..15824071hg19UCSC Ensembl
Innerchr19:15641041..15685071hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3844031
hg1944031
hg1844031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3446n100
Supporting Variantsnssv3564865, nssv3564874, nssv3564866, nssv3564869, nssv3564867, nssv3564875, nssv3564870, nssv3564864, nssv3564873, nssv3564871, nssv3564872, nssv3564868
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)nsv1057902
Frequency
Sample Size29084
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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