A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766336



Internal ID20542196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8588122..8588122hg38UCSC Ensembl
chr2:8728252..8728252hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766336
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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