A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942599



Internal ID22718039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863278..106538610hg38UCSC Ensembl
chr14:106329488..106994612hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38675333
hg19665125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n209
Supporting Variantsnssv17377649
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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