A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103150



Internal ID22012384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46145758..46145758hg38UCSC Ensembl
chr21:47565672..47565672hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645838
Samples
Known GenesFTCD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103150
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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