A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933438



Internal ID22708751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49524700..49525109hg38UCSC Ensembl
chr14:49991418..49991827hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933438
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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