A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110494



Internal ID22019727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72670872..74090670hg38UCSC Ensembl
chr15:72963213..74383011hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381419799
hg191419799
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604211
Samples
Known GenesADPGK, ADPGK-AS1, BBS4, C15orf59, C15orf60, CD276, GOLGA6A, HCN4, HIGD2B, LOXL1, LOXL1-AS1, NEO1, NPTN, NPTN-IT1, PML, STOML1, TBC1D21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110494
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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