A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513913



Internal ID290422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74266718..74267393hg38UCSC Ensembl
chr14:74733421..74734096hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513913
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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