A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423028



Internal ID202054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14496576..14496675hg38UCSC Ensembl
chr1:14823072..14823171hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423028
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