A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058512



Internal ID19147731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669231..15722633hg38UCSC Ensembl
Innerchr19:15780041..15833443hg19UCSC Ensembl
Innerchr19:15641041..15694443hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3853403
hg1953403
hg1853403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3447n100
Supporting Variantsnssv3564929, nssv3564927, nssv3564932, nssv3564930, nssv3564928, nssv3723293, nssv3564926, nssv3564931
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)nsv1058512
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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