A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060296



Internal ID21969461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159304293..159304293hg38UCSC Ensembl
chr1:159274083..159274083hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529936
Samples
Known GenesFCER1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060296
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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