A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155576



Internal ID22086081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40842964..40845088hg38UCSC Ensembl
Outerchr19:40839253..40846478hg38UCSC Ensembl
Innerchr19:41348869..41350993hg19UCSC Ensembl
Outerchr19:41345158..41352383hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg387226
hg197226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013549, nssv4013548
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155576
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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