A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260785



Internal ID20470003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66724690..66725216hg38UCSC Ensembl
chr11:66492161..66492687hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260785
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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