A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024012



Internal ID83719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90637547..90637729hg38UCSC Ensembl
chr9:93399829..93400011hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479938
Supporting Variants
Samples
Known GenesDIRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024012
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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