A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580026



Internal ID21772069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77490306..77490478hg38UCSC Ensembl
chr11:77201351..77201523hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034105
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580026
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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