A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945225



Internal ID22720699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106185769..106875402hg38UCSC Ensembl
chr14:106642431..107283610hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38689634
hg19641180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373455
Samples
Known GenesLINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945225
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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