A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490196



Internal ID267456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9159813..9160393hg38UCSC Ensembl
chr9:9159813..9160393hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021191
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490196
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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