A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744015



Internal ID18718261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107271175..107273155hg38UCSC Ensembl
Outerchr9:107271011..107273334hg38UCSC Ensembl
Innerchr9:110033456..110035436hg19UCSC Ensembl
Outerchr9:110033292..110035615hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382324
hg192324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744015
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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