A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601254



Internal ID6641511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86267577..86268474hg38UCSC Ensembl
Innerchr4:86267597..86268454hg38UCSC Ensembl
Outerchr4:86267557..86268494hg38UCSC Ensembl
chr4:87188730..87189627hg19UCSC Ensembl
Innerchr4:87188750..87189607hg19UCSC Ensembl
Outerchr4:87188710..87189647hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11526913
SamplesNA20763
Known GenesMAPK10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601254
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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