A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082528



Internal ID21498948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28904815..28909250hg38UCSC Ensembl
chr13:29478952..29483387hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg384436
hg194436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585746
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082528
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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