A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930755



Internal ID22706027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863188..106775211hg38UCSC Ensembl
chr14:106329398..107183450hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38912024
hg19854053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647n209
Supporting Variantsnssv17370212
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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