A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415028



Internal ID194292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42745499..42745662hg38UCSC Ensembl
chr1:43211170..43211333hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415028
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer