A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083977



Internal ID21993210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54203800..54203800hg38UCSC Ensembl
chr14:54670518..54670518hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605310
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083977
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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