A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496856



Internal ID273922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93417511..93422395hg38UCSC Ensembl
chr14:93883857..93888741hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg384885
hg194885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699519
Samples
Known GenesUNC79
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496856
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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