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esv2635642

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,209

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):69,285,419-69,286,627Question Mark
Overlapping variant regions from other studies: 143 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):69,679,199-69,680,407Question Mark
Overlapping variant regions from other studies: 21 SVs from 8 studies. See in: genome view    
Submitted genomic67,965,466-67,966,674Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2635642RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1269,285,41969,286,627
esv2635642RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1269,679,19969,680,407
esv2635642Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000012.10Chr1267,965,46667,966,674

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5218720insertionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5218720RemappedPerfectNC_000012.12:g.(69
285419_?)_(?_69286
627)ins?
GRCh38.p12First PassNC_000012.12Chr1269,285,41969,286,627
essv5218720RemappedPerfectNC_000012.11:g.(69
679199_?)_(?_69680
407)ins?
GRCh37.p13First PassNC_000012.11Chr1269,679,19969,680,407
essv5218720Submitted genomicNC_000012.10:g.(67
965466_?)_(?_67966
674)ins?
NCBI36 (hg18)NC_000012.10Chr1267,965,46667,966,674

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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