A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939437



Internal ID22714831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76347430..76347864hg38UCSC Ensembl
chr14:76813773..76814207hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388879
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939437
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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