A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2439266



Internal ID8156138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13062995..13063274hg38UCSC Ensembl
Outerchr10:13062087..13064236hg38UCSC Ensembl
Innerchr10:13104995..13105274hg19UCSC Ensembl
Outerchr10:13104087..13106236hg19UCSC Ensembl
Innerchr10:13145001..13145280hg18UCSC Ensembl
Outerchr10:13144093..13146242hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382150
hg192150
hg182150
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5192548
SamplesNA18507
Known GenesCCDC3
MethodSequencing
AnalysisInversions are detected using the AB Inversion Tool. When one end of a mate pair maps to the opposite strand of the other, the pair provides evidence of an inversion. Multiple instances in the same area will be a positive call.
PlatformNot specified
CommentsoriginalFile=Yoruban_inv.gff
ReferenceMcKernan_et_al_2009
Pubmed ID19546169
Accession Number(s)esv2439266
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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