A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985353



Internal ID21894696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10902609..10902857hg38UCSC Ensembl
chr2:11042735..11042983hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985353
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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