A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001772



Internal ID6713906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:113102707..113120799hg38UCSC Ensembl
Outerchr9:115864987..115883079hg19UCSC Ensembl
Outerchr9:114904808..114922900hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3818093
hg1918093
hg1818093
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564425
SamplesHuRef
Known GenesFAM225A, FAM225B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001772
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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