A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863619



Internal ID22638554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102216936..102225732hg38UCSC Ensembl
chr12:102610714..102619510hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg388797
hg198797
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863619
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