A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945183



Internal ID22720657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75407798..75408637hg38UCSC Ensembl
chr14:75874501..75875340hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv606n209
Supporting Variantsnssv17389350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945183
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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