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esv1333183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,065

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 177 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):93,136,620-93,142,684Question Mark
Overlapping variant regions from other studies: 177 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):92,869,786-92,875,850Question Mark
Overlapping variant regions from other studies: 47 SVs from 19 studies. See in: genome view    
Submitted genomic92,509,434-92,515,498Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv1333183RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1193,136,62093,142,684
esv1333183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1192,869,78692,875,850
esv1333183Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr1192,509,43492,515,498

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
essv4163036deletionHuRefSequencingSequence alignmentHomozygous780,358

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv4163036RemappedPerfectNC_000011.10:g.931
36620_93142684del
GRCh38.p12First PassNC_000011.10Chr1193,136,62093,142,684
essv4163036RemappedPerfectNC_000011.9:g.9286
9786_92875850del
GRCh37.p13First PassNC_000011.9Chr1192,869,78692,875,850
essv4163036Submitted genomicNC_000011.8:g.9250
9434_92515498del
NCBI36 (hg18)NC_000011.8Chr1192,509,43492,515,498

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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