A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697576



Internal ID121242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85546019..85546106hg38UCSC Ensembl
chr14:86012363..86012450hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511217
Supporting Variants
Samples
Known GenesFLRT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697576
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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