A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764820



Internal ID20540680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57293521..57293521hg38UCSC Ensembl
chr14:57760239..57760239hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764820
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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