A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283775



Internal ID20492993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37089894..37089951hg38UCSC Ensembl
chr13:37664031..37664088hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732820
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283775
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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