A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762932



Internal ID18390492
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 StatusS
Merged Variantsesv3564185
Supporting Variants
Samples
Known GenesMAPK10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762932
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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