A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647329



Internal ID21595634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45540162..45540162hg38UCSC Ensembl
chr13:46114297..46114297hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090870
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647329
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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