A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860190



Internal ID22635125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3788568..3802217hg38UCSC Ensembl
chr12:3897734..3911383hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3813650
hg1913650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860190
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