A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564942



Internal ID18419332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166083170..166083676hg38UCSC Ensembl
Outerchr4:166083140..166083789hg38UCSC Ensembl
Innerchr4:167004322..167004828hg19UCSC Ensembl
Outerchr4:167004292..167004941hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763689
Samples
Known GenesTLL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564942
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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