A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939722



Internal ID22715120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863250..106627249hg38UCSC Ensembl
chr14:106329460..107083254hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38764000
hg19753795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n209
Supporting Variantsnssv17374283
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939722
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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