A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594217



Internal ID21786260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28921097..28921173hg38UCSC Ensembl
chr11:28942644..28942720hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594217
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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