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esv2510521

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,204

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 291 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):60,474,495-60,475,698Question Mark
Overlapping variant regions from other studies: 290 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):60,460,228-60,461,431Question Mark
Overlapping variant regions from other studies: 66 SVs from 17 studies. See in: genome view    
Submitted genomic60,435,268-60,436,471Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2510521RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr360,474,49560,475,698
esv2510521RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr360,460,22860,461,431
esv2510521Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr360,435,26860,436,471

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5177784insertionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5177784RemappedPerfectNC_000003.12:g.(60
474495_?)_(?_60475
698)ins?
GRCh38.p12First PassNC_000003.12Chr360,474,49560,475,698
essv5177784RemappedPerfectNC_000003.11:g.(60
460228_?)_(?_60461
431)ins?
GRCh37.p13First PassNC_000003.11Chr360,460,22860,461,431
essv5177784Submitted genomicNC_000003.10:g.(60
435268_?)_(?_60436
471)ins?
NCBI36 (hg18)NC_000003.10Chr360,435,26860,436,471

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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