A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038212



Internal ID21947555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65716403..65716663hg38UCSC Ensembl
chr14:66183121..66183381hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609804
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038212
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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