A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601879



Internal ID21793926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127874887..127874939hg38UCSC Ensembl
chr11:127744782..127744834hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039017
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601879
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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