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esv2635288

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,230

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 176 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):202,544,602-202,545,831Question Mark
Overlapping variant regions from other studies: 176 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):203,409,325-203,410,554Question Mark
Overlapping variant regions from other studies: 59 SVs from 12 studies. See in: genome view    
Submitted genomic203,117,570-203,118,799Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2635288RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2202,544,602202,545,831
esv2635288RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2203,409,325203,410,554
esv2635288Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000002.10Chr2203,117,570203,118,799

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5242828insertionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5242828RemappedPerfectNC_000002.12:g.(20
2544602_?)_(?_2025
45831)ins?
GRCh38.p12First PassNC_000002.12Chr2202,544,602202,545,831
essv5242828RemappedPerfectNC_000002.11:g.(20
3409325_?)_(?_2034
10554)ins?
GRCh37.p13First PassNC_000002.11Chr2203,409,325203,410,554
essv5242828Submitted genomicNC_000002.10:g.(20
3117570_?)_(?_2031
18799)ins?
NCBI36 (hg18)NC_000002.10Chr2203,117,570203,118,799

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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