A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260694



Internal ID20469912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128033017..128033153hg38UCSC Ensembl
chr11:127902912..127903048hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260694
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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