A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589140



Internal ID21781183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36055106..36055106hg38UCSC Ensembl
chr11:36076656..36076656hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093971
Supporting Variants
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589140
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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