A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693899



Internal ID117565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22449120..22531440hg38UCSC Ensembl
chr14:22918112..23000390hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3882321
hg1982279
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147260
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693899
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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