A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716568



Internal ID140234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21979908..21980055hg38UCSC Ensembl
chr18:19559869..19560016hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716568
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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