A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104399



Internal ID22013632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44037960..44037960hg38UCSC Ensembl
chr21:45457841..45457841hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648812
Samples
Known GenesTRAPPC10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104399
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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