A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945690



Internal ID22721170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65426743..65426832hg38UCSC Ensembl
chr14:65893461..65893550hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389174
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945690
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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