A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136808



Internal ID21417573
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 StatusS
Merged Variantsnsv5573827
Supporting Variants
SamplesHG00731
Known GenesMAPK10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136808
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