A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091319



Internal ID21491856
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 StatusS
Merged Variantsnsv5604360
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091319
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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