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esv2569789

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,575

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 235 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):77,617,833-77,619,407Question Mark
Overlapping variant regions from other studies: 235 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):77,910,175-77,911,749Question Mark
Overlapping variant regions from other studies: 77 SVs from 18 studies. See in: genome view    
Submitted genomic75,697,230-75,698,804Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2569789RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1577,617,83377,619,407
esv2569789RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1577,910,17577,911,749
esv2569789Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000015.8Chr1575,697,23075,698,804

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5266481deletionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5266481RemappedPerfectNC_000015.10:g.(77
617833_?)_(?_77619
407)del
GRCh38.p12First PassNC_000015.10Chr1577,617,83377,619,407
essv5266481RemappedPerfectNC_000015.9:g.(779
10175_?)_(?_779117
49)del
GRCh37.p13First PassNC_000015.9Chr1577,910,17577,911,749
essv5266481Submitted genomicNC_000015.8:g.(756
97230_?)_(?_756988
04)del
NCBI36 (hg18)NC_000015.8Chr1575,697,23075,698,804

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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