A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654576



Internal ID21602881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112164017..112164017hg38UCSC Ensembl
chr13:112818331..112818331hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094777
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654576
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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