A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264701



Internal ID20473919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95322047..95322047hg38UCSC Ensembl
chr11:95055211..95055211hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264701
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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