A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026111



Internal ID85140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89187331..89187405hg38UCSC Ensembl
chr9:91802246..91802320hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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