A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614462



Internal ID21806509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126138089..126138167hg38UCSC Ensembl
chr11:126007984..126008062hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614462
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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