A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388058



Internal ID22445928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863860..106537806hg38UCSC Ensembl
chr14:106330070..106993808hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38673947
hg19663739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933466
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388058
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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