A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614609



Internal ID21806656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118331166..118331166hg38UCSC Ensembl
chr11:118201881..118201881hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614609
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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