A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657093



Internal ID21605398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79025048..79025048hg38UCSC Ensembl
chr13:79599183..79599183hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg386052
hg196052
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087713
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657093
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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