A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376380



Internal ID22602049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97703151..97709890hg38UCSC Ensembl
chr13:98355405..98362144hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg386740
hg196740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933956
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376380
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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