A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579122



Internal ID21771165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28615508..28644951hg38UCSC Ensembl
chr11:28637055..28666498hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3829444
hg1929444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022674
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579122
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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