A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001859



Internal ID7066978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123976462..123995054hg38UCSC Ensembl
Outerchr9:126738741..126757333hg19UCSC Ensembl
Outerchr9:125778562..125797154hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3818593
hg1918593
hg1818593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564048
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001859
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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