A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766699



Internal ID20542559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26851331..26851331hg38UCSC Ensembl
chr2:27074199..27074199hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276149
Samples
Known GenesDPYSL5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766699
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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