A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985071



Internal ID21894414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100037440..100037586hg38UCSC Ensembl
chr2:100653902..100654048hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517544
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985071
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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