A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723453



Internal ID147119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40891913..41061696hg38UCSC Ensembl
chr19:41397818..41567601hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38169784
hg19169784
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555857
Supporting Variants
Samples
Known GenesCYP2B6, CYP2B7P, CYP2G1P
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723453
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.158289


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