A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614979



Internal ID21807026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121682744..121693819hg38UCSC Ensembl
chr11:121553452..121564527hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3811076
hg1911076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040372
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614979
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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