A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716802



Internal ID140468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26437607..26441044hg38UCSC Ensembl
chr18:24017571..24021008hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383438
hg193438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716802
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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