A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17019704



Internal ID80777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9838304..9950390hg38UCSC Ensembl
chr9:9838304..9950390hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38112087
hg19112087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484587
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17019704
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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