A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989759



Internal ID21899102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66747912..66775089hg38UCSC Ensembl
chr2:66975044..67002221hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3827178
hg1927178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989759
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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