A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405529



Internal ID22463399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40902446..41047894hg38UCSC Ensembl
chr19:41408351..41553799hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38145449
hg19145449
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975840
Supporting Variants
Samples
Known GenesCYP2B6, CYP2B7P
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405529
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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