A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036296



Internal ID21945639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66959235..66959828hg38UCSC Ensembl
chr11:66726706..66727299hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036296
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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