A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662503



Internal ID21610808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26827471..26827471hg38UCSC Ensembl
chr13:27401608..27401608hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098520
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662503
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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