A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098576



Internal ID21450353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113752129..113752248hg38UCSC Ensembl
chr13:114455102..114455221hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597937
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098576
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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