A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986176



Internal ID21895519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143837150..143837216hg38UCSC Ensembl
chr2:144594719..144594785hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986176
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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