A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565795



Internal ID7037177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:14318225..14338871hg38UCSC Ensembl
Outerchr9:14318224..14338870hg19UCSC Ensembl
Outerchr9:14308224..14328870hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3820647
hg1920647
hg1820647
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991653
Supporting Variants
SamplesHuRef
Known GenesNFIB
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565795
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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