A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144946



Internal ID344151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89360639..89362747hg38UCSC Ensembl
chr14:89826983..89829091hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg382109
hg192109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697131
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144946
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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