A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969051



Internal ID22743986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40880763..41089853hg38UCSC Ensembl
chr19:41386668..41595758hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38209091
hg19209091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1040n209
Supporting Variantsnssv17402922
Samples
Known GenesCYP2A13, CYP2A7, CYP2B6, CYP2B7P, CYP2G1P
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969051
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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