A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17718864



Internal ID142530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:64359518..64421461hg38UCSC Ensembl
chr18:62026753..62088696hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3861944
hg1961944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518038
Supporting Variants
Samples
Known GenesLOC284294
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17718864
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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