A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020970



Internal ID81620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1753431..1780677hg38UCSC Ensembl
chr9:1753431..1780677hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3827247
hg1927247
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147293
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020970
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.005465


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