A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013549



Internal ID22075180
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155576
Supporting Variants
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013549
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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