A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591085



Internal ID21783128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16768991..16770572hg38UCSC Ensembl
chr11:16790538..16792119hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034701
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591085
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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