A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027095



Internal ID21936438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36536921..36557635hg38UCSC Ensembl
chr11:36558471..36579185hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3820715
hg1920715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585608
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027095
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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