A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761788



Internal ID18736034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:187108918..187109167hg38UCSC Ensembl
Outerchr3:187108849..187109219hg38UCSC Ensembl
Innerchr3:186826706..186826955hg19UCSC Ensembl
Outerchr3:186826637..186827007hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563041
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761788
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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