A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935086



Internal ID22710422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41002828..41016461hg38UCSC Ensembl
chr14:41472033..41485666hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3813634
hg1913634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370966
Samples
Known GenesLOC644919
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935086
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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