A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590006



Internal ID21538574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125405047..125405109hg38UCSC Ensembl
chr10:127093616..127093678hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067636
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590006
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