A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563516



Internal ID18764592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:20406126..20406867hg38UCSC Ensembl
Outerchr4:20405899..20406995hg38UCSC Ensembl
Innerchr4:20407749..20408490hg19UCSC Ensembl
Outerchr4:20407522..20408618hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381097
hg191097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762263
Samples
Known GenesSLIT2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563516
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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