A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025199



Internal ID84531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108363481..108369561hg38UCSC Ensembl
chr9:111125761..111131841hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg386081
hg196081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025199
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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