A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945475



Internal ID22720953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39450270..39452134hg38UCSC Ensembl
chr14:39919474..39921338hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg381865
hg191865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945475
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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