A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609097



Internal ID21801144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41429705..41442566hg38UCSC Ensembl
chr13:42003841..42016702hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3812862
hg1912862
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109545
Supporting Variants
Samples
Known GenesOR7E37P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609097
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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