A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691415



Internal ID115081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77430392..77430818hg38UCSC Ensembl
chr13:78004527..78004953hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691415
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.387474


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