A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715444



Internal ID139110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11609159..11614766hg38UCSC Ensembl
chr18:11609158..11614765hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg385608
hg195608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522895
Supporting Variants
Samples
Known GenesSLC35G4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002822


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