A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043447



Internal ID21952751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165914657..165914657hg38UCSC Ensembl
chr2:166771167..166771167hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527843
Samples
Known GenesTTC21B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043447
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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