A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717323



Internal ID140989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35687358..35687409hg38UCSC Ensembl
chr18:33267322..33267373hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560879
Supporting Variants
Samples
Known GenesGALNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717323
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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