A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5394584



Internal ID174013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167536857..167536857hg38UCSC Ensembl
chr1:167506094..167506094hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16892075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5394584
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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