A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989585



Internal ID21898928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5706116..5706266hg38UCSC Ensembl
chr2:5846248..5846398hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989585
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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