A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274373



Internal ID20483591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26481980..26482118hg38UCSC Ensembl
chr13:27056117..27056255hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738502
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274373
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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