A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260621



Internal ID20469839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79499654..79499654hg38UCSC Ensembl
chr11:79210698..79210698hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260621
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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