A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696991



Internal ID120657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38189713..38196637hg38UCSC Ensembl
chr14:38658918..38665842hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg386925
hg196925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696991
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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