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esv3757809

  • Study:estd192 (COSMIC)
  • Variant Type:inversion
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,271

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 190 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):74,653,810-74,656,080Question Mark
Overlapping variant regions from other studies: 190 SVs from 38 studies. See in: genome view    
Submitted genomic72,649,949-72,652,219Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3757809RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1774,653,81074,654,21074,655,68074,656,080
esv3757809Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1772,649,94972,650,34972,651,81972,652,219

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16581090deletion749716CuratedCurated63

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16581090RemappedPerfectNC_000017.11:g.(74
653810_74654210)_(
74655680_74656080)
del
GRCh38.p12First PassNC_000017.11Chr1774,653,81074,654,21074,655,68074,656,080
essv16581090Submitted genomicNC_000017.10:g.(72
649949_72650349)_(
72651819_72652219)
del
GRCh37 (hg19)NC_000017.10Chr1772,649,94972,650,34972,651,81972,652,219

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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