A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17719767



Internal ID143433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78178142..78203273hg38UCSC Ensembl
chr18:75938142..75963273hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3825132
hg1925132
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555789
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17719767
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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