A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108014



Internal ID22017249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45382475..46460727hg38UCSC Ensembl
chr13:45956610..47034862hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381078253
hg191078253
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605278
Samples
Known GenesCOG3, CPB2, CPB2-AS1, FAM194B, KIAA0226L, LCP1, LINC00563, LRRC63, SIAH3, SLC25A30, SPERT, TPT1-AS1, ZC3H13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108014
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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