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esv2538891

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,163

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1277 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):24,499,600-24,538,762Question Mark
Overlapping variant regions from other studies: 1277 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):24,744,747-24,783,909Question Mark
Overlapping variant regions from other studies: 586 SVs from 26 studies. See in: genome view    
Submitted genomic22,295,840-22,335,002Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2538891RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1524,499,60024,538,762
esv2538891RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1524,744,74724,783,909
esv2538891Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000015.8Chr1522,295,84022,335,002

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5249926copy number lossNA18507SequencingRead depth232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5249926RemappedPerfectNC_000015.10:g.(?_
24499600)_(2453876
2_?)del
GRCh38.p12First PassNC_000015.10Chr1524,499,60024,538,762
essv5249926RemappedPerfectNC_000015.9:g.(?_2
4744747)_(24783909
_?)del
GRCh37.p13First PassNC_000015.9Chr1524,744,74724,783,909
essv5249926Submitted genomicNC_000015.8:g.(?_2
2295840)_(22335002
_?)del
NCBI36 (hg18)NC_000015.8Chr1522,295,84022,335,002

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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