A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717251



Internal ID140917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34221426..34221566hg38UCSC Ensembl
chr18:31801390..31801530hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528729
Supporting Variants
Samples
Known GenesNOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717251
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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