A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989456



Internal ID21898799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52209922..52422466hg38UCSC Ensembl
chr2:52437060..52649604hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38212545
hg19212545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989456
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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