A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv521n206



Internal ID22755825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9801913..9950390hg38UCSC Ensembl
chr9:9801913..9950390hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38148478
hg19148478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5483352, nsv5484587
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv521n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer