A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431644



Internal ID22489514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9178576..9567681hg38UCSC Ensembl
chr8:9036086..9425191hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38389106
hg19389106
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975603
Supporting Variants
Samples
Known GenesLOC157273, TNKS
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431644
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