A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721998



Internal ID145664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18116342..18116404hg38UCSC Ensembl
chr19:18227152..18227214hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519313
Supporting Variants
Samples
Known GenesMAST3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721998
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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