A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564186



Internal ID18418576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86145219..86145379hg38UCSC Ensembl
Outerchr4:86145200..86145391hg38UCSC Ensembl
Innerchr4:87066372..87066532hg19UCSC Ensembl
Outerchr4:87066353..87066544hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762933
Samples
Known GenesMAPK10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564186
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer