A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5550361



Internal ID323924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79801111..79801161hg38UCSC Ensembl
chr13:80375246..80375296hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5550361
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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