A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16897034



Internal ID172177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14496344..14496459hg38UCSC Ensembl
chr1:14822840..14822955hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16897034
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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