A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651069



Internal ID21599374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27674806..27674806hg38UCSC Ensembl
chr13:28248943..28248943hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099188
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651069
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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