A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562633



Internal ID18417023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141058127..141059831hg38UCSC Ensembl
Outerchr3:141058118..141059841hg38UCSC Ensembl
Innerchr3:140776969..140778673hg19UCSC Ensembl
Outerchr3:140776960..140778683hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381724
hg191724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761380
Samples
Known GenesSPSB4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562633
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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