A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716223



Internal ID139889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10609148..10609950hg38UCSC Ensembl
chr18:10609145..10609947hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716223
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.421948


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