A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692593



Internal ID116259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99566912..99566927hg38UCSC Ensembl
chr13:100219166..100219181hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692593
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.180768


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