A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082551



Internal ID21465352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26845479..26846839hg38UCSC Ensembl
chr13:27419616..27420976hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381361
hg191361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599798
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082551
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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