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esv3794227

  • Study:estd192 (COSMIC)
  • Variant Type:complex chromosomal rearrangement
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:401

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):110,596,530-110,596,930Question Mark
Overlapping variant regions from other studies: 111 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):115,204,447-115,204,847Question Mark
Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
Submitted genomic110,917,733-110,918,133Question Mark
Overlapping variant regions from other studies: 111 SVs from 27 studies. See in: genome view    
Submitted genomic115,525,611-115,526,011Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stopstrand
esv3794227RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6110,596,530110,596,930110,596,530110,596,930
esv3794227RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6115,204,447115,204,847115,204,447115,204,847-
esv3794227Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6110,917,733110,918,133110,917,733110,918,133
esv3794227Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6115,525,611115,526,011115,525,611115,526,011-

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16621632intrachromosomal translocation1126084CuratedCurated246

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stopstrand
essv16621632RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6110,596,530110,596,930110,596,530110,596,930not reported
essv16621632RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6115,204,447115,204,847115,204,447115,204,847-
essv16621632Submitted genomicGRCh37 (hg19)NC_000006.11Chr6110,917,733110,918,133110,917,733110,918,133not reported
essv16621632Submitted genomicGRCh37 (hg19)NC_000006.11Chr6115,525,611115,526,011115,525,611115,526,011-

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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