A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713728



Internal ID137394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53976859..54005627hg38UCSC Ensembl
chr17:52054220..52082988hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3828769
hg1928769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559205
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713728
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.002967


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