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esv3795370

  • 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:2,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 58 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):104,339,450-104,341,450Question Mark
Overlapping variant regions from other studies: 81 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):114,565,572-114,567,572Question Mark
Overlapping variant regions from other studies: 58 SVs from 19 studies. See in: genome view    
Submitted genomic106,099,208-106,101,208Question Mark
Overlapping variant regions from other studies: 81 SVs from 26 studies. See in: genome view    
Submitted genomic115,003,377-115,005,377Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stopstrand
esv3795370RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10104,339,450104,341,450104,339,450104,341,450
esv3795370RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12114,565,572114,567,572114,565,572114,567,572-
esv3795370Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr10106,099,208106,101,208106,099,208106,101,208
esv3795370Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr12115,003,377115,005,377115,003,377115,005,377-

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16622902interchromosomal translocation2120209CuratedCurated35

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stopstrand
essv16622902RemappedPerfectGRCh38.p12First PassNC_000010.11Chr10104,339,450104,341,450104,339,450104,341,450not reported
essv16622902RemappedPerfectGRCh38.p12First PassNC_000012.12Chr12114,565,572114,567,572114,565,572114,567,572-
essv16622902Submitted genomicGRCh37 (hg19)NC_000010.10Chr10106,099,208106,101,208106,099,208106,101,208not reported
essv16622902Submitted genomicGRCh37 (hg19)NC_000012.11Chr12115,003,377115,005,377115,003,377115,005,377-

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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