A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990567



Internal ID61126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164327018..164400829hg38UCSC Ensembl
chr6:164748051..164821862hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3873812
hg1973812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471441
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990567
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