A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438266



Internal ID216834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9785405..9806808hg38UCSC Ensembl
chr2:9925534..9946937hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3821404
hg1921404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438266
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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