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esv3791221

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 145 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):132,084,642-132,084,642Question Mark
Overlapping variant regions from other studies: 145 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):132,084,830-132,084,830Question Mark
Overlapping variant regions from other studies: 67 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):28,100,458-28,100,458Question Mark
Overlapping variant regions from other studies: 98 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):28,200,280-28,200,280Question Mark
Overlapping variant regions from other studies: 146 SVs from 41 studies. See in: genome view    
Submitted genomic132,842,215-132,842,215Question Mark
Overlapping variant regions from other studies: 146 SVs from 41 studies. See in: genome view    
Submitted genomic132,842,403-132,842,403Question Mark
Overlapping variant regions from other studies: 67 SVs from 17 studies. See in: genome view    
Submitted genomic28,323,325-28,323,325Question Mark
Overlapping variant regions from other studies: 98 SVs from 30 studies. See in: genome view    
Submitted genomic28,221,827-28,221,827Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3791221RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2132,084,642132,084,642
esv3791221RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2132,084,830132,084,830
esv3791221RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr228,100,45828,100,458
esv3791221RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1128,200,28028,200,280
esv3791221Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2132,842,215132,842,215
esv3791221Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2132,842,403132,842,403
esv3791221Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr228,323,32528,323,325
esv3791221Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1128,221,82728,221,827

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16578828intrachromosomal translocation1109520CuratedCurated17
essv16640986interchromosomal translocation1109520CuratedCurated17

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
essv16578828RemappedPerfectGRCh38.p12First PassNC_000002.12Chr228,100,45828,100,458-
essv16640986RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2132,084,642132,084,642-
essv16578828RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2132,084,830132,084,830-
essv16640986RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1128,200,28028,200,280not reported
essv16578828Submitted genomicGRCh37 (hg19)NC_000002.11Chr228,323,32528,323,325-
essv16640986Submitted genomicGRCh37 (hg19)NC_000002.11Chr2132,842,215132,842,215-
essv16578828Submitted genomicGRCh37 (hg19)NC_000002.11Chr2132,842,403132,842,403-
essv16640986Submitted genomicGRCh37 (hg19)NC_000011.9Chr1128,221,82728,221,827not reported

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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