A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580881



Internal ID21529376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165920878..165921233hg38UCSC Ensembl
chr1:165890115..165890470hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061064
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580881
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