A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028526



Internal ID86713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121053455..121053634hg38UCSC Ensembl
chr9:123815733..123815912hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028526
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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