A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641186



Internal ID21589491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106672387..106672387hg38UCSC Ensembl
chr6:107120262..107120262hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154303
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641186
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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