A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590176



Internal ID21538745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7083650..7083830hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088619
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590176
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