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esv2509951

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,450

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 377 SVs from 48 studies. See in: genome view    
Remapped(Score: Pass):239,898,361-239,899,810Question Mark
Overlapping variant regions from other studies: 377 SVs from 48 studies. See in: genome view    
Remapped(Score: Pass):240,837,778-240,839,227Question Mark
Overlapping variant regions from other studies: 191 SVs from 12 studies. See in: genome view    
Submitted genomic240,486,792-240,487,935Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2509951RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2239,898,361239,899,810
esv2509951RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2240,837,778240,839,227
esv2509951Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000002.10Chr2240,486,792240,487,935

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5201055insertionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5201055RemappedPassNC_000002.12:g.(23
9898361_?)_(?_2398
99810)ins?
GRCh38.p12First PassNC_000002.12Chr2239,898,361239,899,810
essv5201055RemappedPassNC_000002.11:g.(24
0837778_?)_(?_2408
39227)ins?
GRCh37.p13First PassNC_000002.11Chr2240,837,778240,839,227
essv5201055Submitted genomicNC_000002.10:g.(24
0486792_?)_(?_2404
87935)ins?
NCBI36 (hg18)NC_000002.10Chr2240,486,792240,487,935

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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