A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931113



Internal ID22706392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105864634..106537813hg38UCSC Ensembl
chr14:106330844..106993815hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38673180
hg19662972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n209
Supporting Variantsnssv17372472
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931113
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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