A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445813



Internal ID22503683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8309480..8919987hg38UCSC Ensembl
chr6:8309713..8920220hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38610508
hg19610508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974999
Supporting Variants
Samples
Known GenesHULC, LOC100506207, SLC35B3
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445813
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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