A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397639



Internal ID177044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46039175..46039226hg38UCSC Ensembl
chr3:46080667..46080718hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933275
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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