A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591910



Internal ID21783953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84685270..84879675hg38UCSC Ensembl
chr11:84396313..84590719hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38194406
hg19194407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024735
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591910
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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