A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv198e180



Internal ID22757608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107774927..107778756hg38UCSC Ensembl
chr9:110537208..110541037hg19UCSC Ensembl
chr9:109577029..109580858hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg383830
hg193830
hg183830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv989814, esv990413
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv198e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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