A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611524



Internal ID21803571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91964708..93490522hg38UCSC Ensembl
chr13:92616962..94142775hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381525815
hg191525814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110056
Supporting Variants
Samples
Known GenesGPC5, GPC5-AS1, GPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611524
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer