A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280318



Internal ID20489536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52506525..52506864hg38UCSC Ensembl
chr14:52973243..52973582hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743102
Supporting Variants
Samples
Known GenesTXNDC16
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280318
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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