A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108636



Internal ID22017869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3277634..3420064hg38UCSC Ensembl
chr17:3180928..3323358hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38142431
hg19142431
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621406
Samples
Known GenesOR1E1, OR3A1, OR3A2, OR3A4P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108636
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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