A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564408



Internal ID18765484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107142956..107153031hg38UCSC Ensembl
Outerchr4:107140160..107155572hg38UCSC Ensembl
Innerchr4:108064113..108074188hg19UCSC Ensembl
Outerchr4:108061317..108076729hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3815413
hg1915413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763155
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564408
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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