A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510832



Internal ID287439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77956867..77958125hg38UCSC Ensembl
chr14:78423210..78424468hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510832
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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