A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457699



Internal ID235738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149457903..149493299hg38UCSC Ensembl
chr5:148837466..148872862hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3835397
hg1935397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457699
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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