A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16893627



Internal ID169909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11928444..11933350hg38UCSC Ensembl
chr1:11988501..11993407hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384907
hg194907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16893627
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006717


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