A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498489



Internal ID275481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72800377..72800497hg38UCSC Ensembl
chr14:73267085..73267205hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696052
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498489
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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