A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663900



Internal ID21612205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79607611..79607611hg38UCSC Ensembl
chr13:80181746..80181746hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096298
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663900
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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