A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717485



Internal ID141151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38841033..38846546hg38UCSC Ensembl
chr18:36420997..36426510hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg385514
hg195514
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563866
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717485
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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