A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988709



Internal ID59899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110892346..110892796hg38UCSC Ensembl
chr6:111213549..111213999hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454545
Supporting Variants
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988709
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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