A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564797



Internal ID18765873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151421593..151422285hg38UCSC Ensembl
Outerchr4:151421500..151422325hg38UCSC Ensembl
Innerchr4:152342745..152343437hg19UCSC Ensembl
Outerchr4:152342652..152343477hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763544
Samples
Known GenesFAM160A1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564797
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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