A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424063



Internal ID203066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158824566..158827463hg38UCSC Ensembl
chr1:158794356..158797253hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382898
hg192898
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424063
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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