A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588053



Internal ID21780096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86731549..86731549hg38UCSC Ensembl
chr11:86442591..86442591hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588053
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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