esv1011758

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 31 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):233,236,801-233,236,804Question Mark
Overlapping variant regions from other studies: 31 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):234,145,447-234,145,450Question Mark
Overlapping variant regions from other studies: 29 SVs from 4 studies. See in: genome view    
Submitted genomic233,810,186-233,810,189Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv1011758RemappedPerfectGRCh38Primary AssemblyFirst PassNC_000002.12Chr2233,236,801233,236,804
esv1011758RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000002.11Chr2234,145,447234,145,450
esv1011758Submitted genomicNCBI36 (hg18)NC_000002.10Chr2233,810,186233,810,189

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls from this Sample
essv3726189deletionHuRefSequencingSequence alignmentHeterozygous780,358

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrStartStop
essv3726189RemappedPerfectNC_000002.12:g.233236801_233236804delGRCh38Primary AssemblyFirst PassNC_000002.12Chr2233,236,801233,236,804
essv3726189RemappedPerfectNC_000002.11:g.234145447_234145450delGRCh37 (hg19)Primary AssemblyFirst PassNC_000002.11Chr2234,145,447234,145,450
essv3726189Submitted genomicNC_000002.10:g.233810186_233810189delNCBI36 (hg18)NC_000002.10Chr2233,810,186233,810,189

There are no validations for this variant

There are no clinical assertions for this variant

There is no genotype information for this variant

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