A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454906



Internal ID233000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104186236..104390773hg38UCSC Ensembl
chr6:104634111..104838648hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38204538
hg19204538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454906
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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