A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17718148



Internal ID141814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:51105956..51112498hg38UCSC Ensembl
chr18:48632326..48638868hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg386543
hg196543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17718148
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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