A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087387



Internal ID21996620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102730791..102730791hg38UCSC Ensembl
chr11:102601522..102601522hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381288
hg191288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596897
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087387
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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