A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267333



Internal ID20476551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68372418..68372418hg38UCSC Ensembl
chr11:68139886..68139886hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761867
Supporting Variants
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267333
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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