A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989801



Internal ID21899144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68102939..68126594hg38UCSC Ensembl
chr2:68330071..68353726hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3823656
hg1923656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523803
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989801
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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