A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848080



Internal ID22623015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91150485..91155061hg38UCSC Ensembl
chr12:91544262..91548838hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg384577
hg194577
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466135
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848080
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