A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564185



Internal ID18418575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86055752..86058459hg38UCSC Ensembl
Outerchr4:86055085..86058922hg38UCSC Ensembl
Innerchr4:86976905..86979612hg19UCSC Ensembl
Outerchr4:86976238..86980075hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg383838
hg193838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762932
Samples
Known GenesMAPK10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564185
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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