A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729434



Internal ID153100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44859654..44865976hg38UCSC Ensembl
chr22:45255534..45261856hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg386323
hg196323
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558269
Supporting Variants
Samples
Known GenesARHGAP8, PRR5-ARHGAP8
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729434
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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