A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292241



Internal ID20501459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101230879..101230996hg38UCSC Ensembl
chr11:101101610..101101727hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743180
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292241
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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