A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896499



Internal ID171807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16103253..16108738hg38UCSC Ensembl
chr1:16429748..16435233hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg385486
hg195486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896499
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.029513


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