A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494732



Internal ID271865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87849067..87849202hg38UCSC Ensembl
chr14:88315411..88315546hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494732
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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