A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015884



Internal ID20582924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863240..106810439hg38UCSC Ensembl
chr14:106329450..107218673hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38947200
hg19889224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511415
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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