A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17019697



Internal ID80773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9801913..9929461hg38UCSC Ensembl
chr9:9801913..9929461hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38127549
hg19127549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483352
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17019697
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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