A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082181



Internal ID21449682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73325318..73325318hg38UCSC Ensembl
chr13:73899455..73899455hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646298
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082181
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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