A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930332



Internal ID22705597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39438846..39438928hg38UCSC Ensembl
chr14:39908050..39908132hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930332
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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