A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598429



Internal ID21547056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32596633..32597199hg38UCSC Ensembl
chr13:33170770..33171336hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090886
SamplesNA19238
Known GenesPDS5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598429
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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