A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579592



Internal ID16367001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40875596..40883401hg38UCSC Ensembl
Innerchr19:41381501..41389306hg19UCSC Ensembl
Innerchr19:46073341..46081146hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg387806
hg197806
hg187806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6452n54
Supporting Variantsnssv899515
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579592
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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