A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988188



Internal ID21897531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22898889..22899999hg38UCSC Ensembl
chr2:23121761..23122871hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg381111
hg191111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531851
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988188
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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