A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375832



Internal ID22601501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105864629..106737110hg38UCSC Ensembl
chr14:106330839..107174928hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38872482
hg19844090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946828
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375832
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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