A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565209



Internal ID18766285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186693378..186693657hg38UCSC Ensembl
Outerchr4:186693308..186693715hg38UCSC Ensembl
Innerchr4:187614532..187614811hg19UCSC Ensembl
Outerchr4:187614462..187614869hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763956
Samples
Known GenesFAT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565209
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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