A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928100



Internal ID22703335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103343623..103344375hg38UCSC Ensembl
chr14:103809960..103810712hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373814
Samples
Known GenesEIF5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928100
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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