esv1011748

  • Variant Calls:1
  • 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: 67 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):92,932,151-92,932,151Question Mark
Overlapping variant regions from other studies: 67 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):95,694,433-95,694,433Question Mark
Overlapping variant regions from other studies: 40 SVs from 10 studies. See in: genome view    
Submitted genomic94,734,254-94,734,254Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv1011748RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000009.12Chr992,932,15192,932,151
esv1011748RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000009.11Chr995,694,43395,694,433
esv1011748Submitted genomicNCBI36 (hg18)NC_000009.10Chr994,734,25494,734,254

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
essv3893330insertionHuRefSequencingSequence alignmentHeterozygous780,358

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrStartStop
essv3893330RemappedPerfectNC_000009.12:g.929
32150_92932151insT
GRCh38 (hg38)Primary AssemblyFirst PassNC_000009.12Chr992,932,15192,932,151
essv3893330RemappedPerfectNC_000009.11:g.956
94432_95694433insT
GRCh37 (hg19)Primary AssemblyFirst PassNC_000009.11Chr995,694,43395,694,433
essv3893330Submitted genomicNC_000009.10:g.947
34253_94734254insT
NCBI36 (hg18)NC_000009.10Chr994,734,25494,734,254

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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