A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259827



Internal ID22064437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154312887..154312887hg38UCSC Ensembl
chr3:154030676..154030676hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17855879
Samples
Known GenesDHX36
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259827
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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