A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143776



Internal ID342977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77408106..77414106hg38UCSC Ensembl
chr13:77982241..77988241hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143776
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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