A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029999



Internal ID87720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132648082..132687044hg38UCSC Ensembl
chr9:135523469..135562431hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3838963
hg1938963
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562425
Supporting Variants
Samples
Known GenesDDX31, GTF3C4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029999
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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