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esv2490419

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,803

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 334 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):1,893,463-1,916,265Question Mark
Overlapping variant regions from other studies: 334 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):1,914,693-1,937,495Question Mark
Overlapping variant regions from other studies: 132 SVs from 21 studies. See in: genome view    
Submitted genomic1,871,269-1,894,071Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2490419RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr111,893,4631,916,265
esv2490419RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr111,914,6931,937,495
esv2490419Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr111,871,2691,894,071

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5266279deletionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5266279RemappedPerfectNC_000011.10:g.(18
93463_?)_(?_191626
5)del
GRCh38.p12First PassNC_000011.10Chr111,893,4631,916,265
essv5266279RemappedPerfectNC_000011.9:g.(191
4693_?)_(?_1937495
)del
GRCh37.p13First PassNC_000011.9Chr111,914,6931,937,495
essv5266279Submitted genomicNC_000011.8:g.(187
1269_?)_(?_1894071
)del
NCBI36 (hg18)NC_000011.8Chr111,871,2691,894,071

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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