A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563761



Internal ID18764837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:41225799..41229521hg38UCSC Ensembl
Outerchr4:41225545..41230233hg38UCSC Ensembl
Innerchr4:41227816..41231538hg19UCSC Ensembl
Outerchr4:41227562..41232250hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg384689
hg194689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762508
Samples
Known GenesUCHL1-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563761
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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