A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510634



Internal ID287245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24224224..24224330hg38UCSC Ensembl
chr14:24693430..24693536hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693430
Samples
Known GenesNEDD8, NEDD8-MDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510634
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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