A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697909



Internal ID121575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75313261..75313822hg38UCSC Ensembl
chr14:75779964..75780525hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697909
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001873


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