A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277656



Internal ID20486874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124443015..124443015hg38UCSC Ensembl
chr11:124312911..124312911hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277656
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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