A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716780



Internal ID140446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26053317..26053677hg38UCSC Ensembl
chr18:23633281..23633641hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520968
Supporting Variants
Samples
Known GenesSS18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716780
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009991


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