A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648497



Internal ID21596802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76961647..76961647hg38UCSC Ensembl
chr13:77535782..77535782hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090819
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648497
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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