A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023982



Internal ID83701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88521055..88530694hg38UCSC Ensembl
chr9:91135970..91145609hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg389640
hg199640
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023982
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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