A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496120



Internal ID273206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22965190..22967827hg38UCSC Ensembl
chr14:23434399..23437036hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382638
hg192638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496120
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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