A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427087



Internal ID205999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24018740..24023476hg38UCSC Ensembl
chr1:24345230..24349966hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384737
hg194737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv14n206
Supporting Variantsnssv16901155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427087
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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