A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697854



Internal ID121520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69820560..69831364hg38UCSC Ensembl
chr14:70287277..70298081hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3810805
hg1910805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512425
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697854
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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