A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5404074



Internal ID183432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42856915..42856915hg38UCSC Ensembl
chr3:42898407..42898407hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931932
Samples
Known GenesACKR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5404074
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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