A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762263



Internal ID18736509
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 StatusS
Merged Variantsesv3563516
Supporting Variants
Samples
Known GenesSLIT2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762263
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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