A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091431



Internal ID22000664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79921825..79921825hg38UCSC Ensembl
chr14:80388168..80388168hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091431
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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