A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501269



Internal ID278173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25774318..25774427hg38UCSC Ensembl
chr14:26243524..26243633hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501269
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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