A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573827



Internal ID21522235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86173939..86173998hg38UCSC Ensembl
chr4:87095092..87095151hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136808
SamplesHG00731
Known GenesMAPK10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573827
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