A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265172



Internal ID20474390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126276304..126276304hg38UCSC Ensembl
chr11:126146199..126146199hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750342
Supporting Variants
Samples
Known GenesFOXRED1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265172
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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