A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989007



Internal ID21898350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3590536..3590773hg38UCSC Ensembl
chr2:3638126..3638363hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989007
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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