A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032678



Internal ID21942021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41300323..41310411hg38UCSC Ensembl
chr13:41874459..41884547hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3810089
hg1910089
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032678
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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