A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892860



Internal ID169411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184109693..184109755hg38UCSC Ensembl
chr1:184078827..184078889hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892860
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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