A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693449



Internal ID117115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24531637..24551713hg38UCSC Ensembl
chr14:25000843..25020919hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3820077
hg1920077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693449
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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