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esv1585596

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,052

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 198 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):93,638,303-93,644,354Question Mark
Overlapping variant regions from other studies: 198 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):94,559,454-94,565,505Question Mark
Overlapping variant regions from other studies: 71 SVs from 17 studies. See in: genome view    
Submitted genomic94,778,477-94,784,528Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv1585596RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr493,638,30393,644,354
esv1585596RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr494,559,45494,565,505
esv1585596Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr494,778,47794,784,528

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
essv4015401deletionHuRefSequencingSequence alignmentHomozygous780,358

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv4015401RemappedPerfectNC_000004.12:g.936
38303_93644354del
GRCh38.p12First PassNC_000004.12Chr493,638,30393,644,354
essv4015401RemappedPerfectNC_000004.11:g.945
59454_94565505del
GRCh37.p13First PassNC_000004.11Chr494,559,45494,565,505
essv4015401Submitted genomicNC_000004.10:g.947
78477_94784528del
NCBI36 (hg18)NC_000004.10Chr494,778,47794,784,528

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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