A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441674



Internal ID220137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43034476..43034548hg38UCSC Ensembl
chr2:43261615..43261687hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16911632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441674
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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