A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009770



Internal ID7074064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128131557..128143301hg38UCSC Ensembl
Outerchr9:130893836..130905580hg19UCSC Ensembl
Outerchr9:129933657..129945401hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3811745
hg1911745
hg1811745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565783
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009770
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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