A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941497



Internal ID22716922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105891199..106770576hg38UCSC Ensembl
chr14:106357057..107178818hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38879378
hg19821762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647n209
Supporting Variantsnssv17370384
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941497
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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