A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988915



Internal ID21898258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33276040..33276091hg38UCSC Ensembl
chr2:33501107..33501158hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524444
Samples
Known GenesLTBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988915
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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