A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004259



Internal ID7069359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20422956..22308242hg38UCSC Ensembl
Outerchr15:20628209..22596193hg19UCSC Ensembl
Outerchr15:18888223..20099321hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381885287
hg191967985
hg181211099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565264
SamplesHuRef
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004259
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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