A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487168



Internal ID264512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8796589..8799095hg38UCSC Ensembl
chr9:8796589..8799095hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382507
hg192507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021153
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487168
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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