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esv2577005

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,918

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 259 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):15,329,787-15,340,704Question Mark
Overlapping variant regions from other studies: 259 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):15,310,433-15,321,350Question Mark
Overlapping variant regions from other studies: 68 SVs from 18 studies. See in: genome view    
Submitted genomic15,258,433-15,269,350Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2577005RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2015,329,78715,340,704
esv2577005RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2015,310,43315,321,350
esv2577005Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000020.9Chr2015,258,43315,269,350

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5285755deletionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5285755RemappedPerfectNC_000020.11:g.(15
329787_?)_(?_15340
704)del
GRCh38.p12First PassNC_000020.11Chr2015,329,78715,340,704
essv5285755RemappedPerfectNC_000020.10:g.(15
310433_?)_(?_15321
350)del
GRCh37.p13First PassNC_000020.10Chr2015,310,43315,321,350
essv5285755Submitted genomicNC_000020.9:g.(152
58433_?)_(?_152693
50)del
NCBI36 (hg18)NC_000020.9Chr2015,258,43315,269,350

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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