A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563835



Internal ID18764911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48412319..48412532hg38UCSC Ensembl
Outerchr4:48412294..48412569hg38UCSC Ensembl
Innerchr4:48414336..48414549hg19UCSC Ensembl
Outerchr4:48414311..48414586hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762582
Samples
Known GenesSLAIN2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563835
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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