A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063072



Internal ID19152291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669231..15723148hg38UCSC Ensembl
Innerchr19:15780041..15833958hg19UCSC Ensembl
Innerchr19:15641041..15694958hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3853918
hg1953918
hg1853918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3447n100
Supporting Variantsnssv3564944, nssv3564936, nssv3564940, nssv3564939, nssv3564945, nssv3564943, nssv3564941, nssv3564938, nssv3564937, nssv3564935, nssv3564942
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)nsv1063072
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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