A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259630



Internal ID20468848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53328573..53328648hg38UCSC Ensembl
chr13:53902708..53902783hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259630
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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