A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545106



Internal ID18746182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90233064..90236312hg38UCSC Ensembl
Outerchr9:90233055..90236322hg38UCSC Ensembl
Innerchr9:92995346..92998594hg19UCSC Ensembl
Outerchr9:92995337..92998604hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg383268
hg193268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743853
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545106
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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