A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028682



Internal ID86824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125264843..125265497hg38UCSC Ensembl
chr9:128027122..128027776hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482590
Supporting Variants
Samples
Known GenesGAPVD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028682
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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