A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860734



Internal ID22635669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80784524..80786655hg38UCSC Ensembl
chr12:81178303..81180434hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg382132
hg192132
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860734
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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