A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743893



Internal ID18371453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94613959..94614384hg38UCSC Ensembl
Outerchr9:94613925..94614413hg38UCSC Ensembl
Innerchr9:97376241..97376666hg19UCSC Ensembl
Outerchr9:97376207..97376695hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545146
Supporting Variants
Samples
Known GenesFBP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743893
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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