A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3543995



Internal ID18745071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:108717972..108718255hg38UCSC Ensembl
Outerchr8:108717911..108718301hg38UCSC Ensembl
Innerchr8:109730201..109730484hg19UCSC Ensembl
Outerchr8:109730140..109730530hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742742
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3543995
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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