A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652569



Internal ID21600874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99729936..99729936hg38UCSC Ensembl
chr13:100382190..100382190hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098026
SamplesHG00731
Known GenesCLYBL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652569
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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