A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762582



Internal ID18736828
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 StatusS
Merged Variantsesv3563835
Supporting Variants
Samples
Known GenesSLAIN2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762582
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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