A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290038



Internal ID20499256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106581844..106854530hg38UCSC Ensembl
chr14:107037830..107262745hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38272687
hg19224916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747419
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290038
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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