A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578202



Internal ID21526666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137739828..137740334hg38UCSC Ensembl
chr6:138060965..138061471hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145462
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578202
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