A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901119



Internal ID1555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23869676..23870541hg38UCSC Ensembl
chr1:24196166..24197031hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901119
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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