A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688289



Internal ID111955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60817572..60817690hg38UCSC Ensembl
chr13:61391706..61391824hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688289
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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