A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697920



Internal ID121586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75523919..75534748hg38UCSC Ensembl
chr14:75990262..76001091hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3810830
hg1910830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510249
Supporting Variants
Samples
Known GenesBATF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697920
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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