A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095580



Internal ID22004813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98330536..98330536hg38UCSC Ensembl
chr14:98796873..98796873hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095580
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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