A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988029



Internal ID21897372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235709533..235709592hg38UCSC Ensembl
chr2:236618177..236618236hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537513
Samples
Known GenesAGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988029
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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