A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989814



Internal ID7076399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107775244..107778318hg38UCSC Ensembl
chr9:110537525..110540599hg19UCSC Ensembl
chr9:109577346..109580420hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg383075
hg193075
hg183075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv198e180
Supporting Variantsessv3580184
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989814
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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