A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592979



Internal ID21785022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80356922..80357190hg38UCSC Ensembl
chr11:80067966..80068234hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031448
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592979
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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