A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028659



Internal ID86805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125163718..125168997hg38UCSC Ensembl
chr9:127925997..127931276hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385280
hg195280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493716
Supporting Variants
Samples
Known GenesPPP6C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028659
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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