A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080990



Internal ID21990223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35604444..35604444hg38UCSC Ensembl
chr11:35625992..35625992hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080990
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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