A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283005



Internal ID20492223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51911626..51912186hg38UCSC Ensembl
chr14:52378344..52378904hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736281
Supporting Variants
Samples
Known GenesGNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283005
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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