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esv23382

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:838

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 170 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):33,621,577-33,622,414Question Mark
Overlapping variant regions from other studies: 170 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):34,112,483-34,113,320Question Mark
Overlapping variant regions from other studies: 73 SVs from 10 studies. See in: genome view    
Submitted genomic38,804,323-38,805,160Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv23382RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1933,621,57733,622,414
esv23382RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1934,112,48334,113,320
esv23382Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000019.8Chr1938,804,32338,805,160

Variant Call Information

Variant Call IDTypeMethod
esv11860copy number variationMerged region

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrInner StartInner Stop
esv11860RemappedPerfectGRCh38.p12First PassNC_000019.10Chr1933,621,57733,622,414
esv11860RemappedPerfectGRCh37.p13First PassNC_000019.9Chr1934,112,48334,113,320
esv11860Submitted genomicNCBI36 (hg18)NC_000019.8Chr1938,804,32338,805,160

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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