A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039355



Internal ID21948698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24220020..24284207hg38UCSC Ensembl
chr11:24241566..24305753hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3864188
hg1964188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039355
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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