A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698067



Internal ID121733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62177794..62212085hg38UCSC Ensembl
chr14:62644512..62678803hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3834292
hg1934292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698067
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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