A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409194



Internal ID188516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24856160..24856211hg38UCSC Ensembl
chr6:24856388..24856439hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735504
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409194
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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