A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989224



Internal ID21898567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43510869..43521109hg38UCSC Ensembl
chr2:43738008..43748248hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3810241
hg1910241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530030
Samples
Known GenesTHADA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989224
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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