A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989669



Internal ID21899012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42903889..42911020hg38UCSC Ensembl
chr2:43131029..43138160hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg387132
hg197132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989669
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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