A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925107



Internal ID21345176
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 Variantsnssv15183838
SamplesHG002
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925107
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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