A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935793



Internal ID22711138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75407746..75408747hg38UCSC Ensembl
chr14:75874449..75875450hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv606n209
Supporting Variantsnssv17380902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935793
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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