A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589861



Internal ID21781904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86024251..86024251hg38UCSC Ensembl
chr11:85735294..85735294hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082770
Supporting Variants
Samples
Known GenesPICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589861
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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