A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2559743



Internal ID8623301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:31506033..31527604hg38UCSC Ensembl
Outerchr1:31498644..31528029hg38UCSC Ensembl
Innerchr1:31971633..31993205hg19UCSC Ensembl
Outerchr1:31971485..31993630hg19UCSC Ensembl
Innerchr1:31744220..31765792hg18UCSC Ensembl
Outerchr1:31744072..31766217hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3829386
hg1922146
hg1822146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5234776
SamplesNA18507
Known GenesLOC149086, LOC284551
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)esv2559743
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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