A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100571



Internal ID22009804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52366326..52481797hg38UCSC Ensembl
chr13:52940461..53055932hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38115472
hg19115472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616531
Samples
Known GenesCKAP2, THSD1, VPS36
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100571
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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