A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086966



Internal ID21482783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109383166..109383166hg38UCSC Ensembl
chr13:110035513..110035513hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658317
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086966
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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