A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599646



Internal ID21791692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129658710..129795992hg38UCSC Ensembl
chr11:129528605..129665887hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38137283
hg19137283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599646
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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