A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5403153



Internal ID182516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28168810..28168861hg38UCSC Ensembl
chr8:28026327..28026378hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17010130
Samples
Known GenesELP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5403153
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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