A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031825



Internal ID21941168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65692387..65692442hg38UCSC Ensembl
chr14:66159105..66159160hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601111
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031825
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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