A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026267



Internal ID21935610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45119420..45119706hg38UCSC Ensembl
chr14:45588623..45588909hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610195
Samples
Known GenesFKBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026267
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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