A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642946



Internal ID21591251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108523978..108523978hg38UCSC Ensembl
chr6:108845181..108845181hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155487
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642946
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