A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267803



Internal ID20477021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112213891..112213891hg38UCSC Ensembl
chr11:112084614..112084614hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758136
Supporting Variants
Samples
Known GenesBCO2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267803
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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