A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039796



Internal ID21949139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65734873..65734951hg38UCSC Ensembl
chr11:65502344..65502422hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039796
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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