A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027682



Internal ID21937025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25246521..25398214hg38UCSC Ensembl
chr14:25715727..25867420hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38151694
hg19151694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027682
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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