A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084221



Internal ID21993454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100345050..100345050hg38UCSC Ensembl
chr14:100811387..100811387hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600260
Samples
Known GenesWARS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084221
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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