A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991245



Internal ID61563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997679..166998135hg38UCSC Ensembl
chr6:167411167..167411623hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141505
Supporting Variants
Samples
Known GenesMIR3939
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991245
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.109741


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