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esv3689113

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 394 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):1,176,279-1,176,279Question Mark
Overlapping variant regions from other studies: 27 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):34,833-34,833Question Mark
Overlapping variant regions from other studies: 394 SVs from 35 studies. See in: genome view    
Submitted genomic1,126,279-1,126,279Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3689113RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr81,176,2791,176,279
esv3689113RemappedPerfectGRCh38.p12ALT_REF_LOCI_2Second PassNT_187655.1Chr8|NT_18
7655.1
34,83334,833
esv3689113Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr81,126,2791,126,279

Variant Call Information

Variant Call IDTypeMethodAnalysis
essv16473280insertionSequencingde novo sequence assembly

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv16473280RemappedPerfectNT_187655.1:g.3483
3_34834ins147
GRCh38.p12Second PassNT_187655.1Chr8|NT_18
7655.1
34,83334,833
essv16473280RemappedPerfectNC_000008.11:g.117
6279_1176280ins147
GRCh38.p12First PassNC_000008.11Chr81,176,2791,176,279
essv16473280Submitted genomicNC_000008.10:g.112
6279_1126280ins147
GRCh37 (hg19)NC_000008.10Chr81,126,2791,126,279

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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