A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281033



Internal ID20490251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159304297..159304297hg38UCSC Ensembl
chr1:159274087..159274087hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759214
Supporting Variants
Samples
Known GenesFCER1A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281033
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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