A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990033



Internal ID60764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154357633..154360426hg38UCSC Ensembl
chr6:154678767..154681560hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382794
hg192794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462759
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990033
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