A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505528



Internal ID282299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59366135..59366328hg38UCSC Ensembl
chr14:59832853..59833046hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17695928
Samples
Known GenesDAAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505528
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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