A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583229



Internal ID21531751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108369599..108377438hg38UCSC Ensembl
chr6:108690803..108698642hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg387840
hg197840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147553
SamplesHG03486
Known GenesLACE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583229
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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