A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021113



Internal ID21930456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83431041..83436119hg38UCSC Ensembl
chr11:83142084..83147162hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385079
hg195079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021113
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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