A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604360



Internal ID21553028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110813041..110813216hg38UCSC Ensembl
chr13:111465388..111465563hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091319
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604360
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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