A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103308



Internal ID22012541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29130040..29130971hg38UCSC Ensembl
chr13:29704177..29705108hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612923
Samples
Known GenesMTUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103308
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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