A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687896



Internal ID111562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:54127699..54133060hg38UCSC Ensembl
chr13:54701834..54707195hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg385362
hg195362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508439
Supporting Variants
Samples
Known GenesLINC00458
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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