A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687992



Internal ID111658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:55874907..55971951hg38UCSC Ensembl
chr13:56449041..56546085hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3897045
hg1997045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687992
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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