A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058037



Internal ID19147256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15542560..15619666hg38UCSC Ensembl
Innerchr19:15653371..15730477hg19UCSC Ensembl
Innerchr19:15514371..15591477hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3877107
hg1977107
hg1877107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3443n100
Supporting Variantsnssv3564795
Samples
Known GenesCYP4F22, CYP4F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058037
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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