A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564767



Internal ID18765843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148178433..148180333hg38UCSC Ensembl
Outerchr4:148178103..148180488hg38UCSC Ensembl
Innerchr4:149099584..149101484hg19UCSC Ensembl
Outerchr4:149099254..149101639hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg382386
hg192386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763514
Samples
Known GenesNR3C2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564767
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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