A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090886



Internal ID21491447
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 StatusS
Merged Variantsnsv5598429
Supporting Variants
SamplesNA19238
Known GenesPDS5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090886
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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