A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598739



Internal ID21790784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133542178..133546973hg38UCSC Ensembl
chr11:133412073..133416868hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384796
hg194796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598739
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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