A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448579



Internal ID22114756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65692459..65692509hg38UCSC Ensembl
chr14:66159177..66159227hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762879
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448579
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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