A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602413



Internal ID21794460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118331102..118331280hg38UCSC Ensembl
chr11:118201817..118201995hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028700
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602413
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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