A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091423



Internal ID21491869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111669489..111669611hg38UCSC Ensembl
chr13:112321836..112321958hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592975
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091423
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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