A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686559



Internal ID110225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29853014..29873858hg38UCSC Ensembl
chr13:30427151..30447995hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3820845
hg1920845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504697
Supporting Variants
Samples
Known GenesLINC00297
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686559
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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