A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499569



Internal ID276537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96577919..96577976hg38UCSC Ensembl
chr14:97044256..97044313hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499569
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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