A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108082



Internal ID22017316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18831464..18877797hg38UCSC Ensembl
chr13:19405604..19451937hg19UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3846334
hg1946334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604460
Samples
Known GenesANKRD20A9P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108082
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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