A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985397



Internal ID57672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90030589..90104973hg38UCSC Ensembl
chr6:90740308..90814692hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3874385
hg1974385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457353
Supporting Variants
Samples
Known GenesBACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985397
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