A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278088



Internal ID20487306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78659292..78659292hg38UCSC Ensembl
chr13:79233427..79233427hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762685
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278088
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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