A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276972



Internal ID20486190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110930789..110930789hg38UCSC Ensembl
chr11:110801513..110801513hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276972
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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