A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766980



Internal ID20542840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127119463..127119463hg38UCSC Ensembl
chr2:127877039..127877039hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766980
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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