A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983386



Internal ID56299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57224186..57235069hg38UCSC Ensembl
chr6:57088984..57099867hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg3810884
hg1910884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983386
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