A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986962



Internal ID58758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97323214..97323417hg38UCSC Ensembl
chr6:97771090..97771293hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455038
Supporting Variants
Samples
Known GenesMIR548H3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986962
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