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nsv4768286

  • 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: 129 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):66,336,672-66,336,672Question Mark
Overlapping variant regions from other studies: 129 SVs from 21 studies. See in: genome view    
Submitted genomic64,332,790-64,332,790Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4768286RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1766,336,67266,336,672
nsv4768286Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1764,332,79064,332,790

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16269535insertionSequencingSplit read mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16269535RemappedPerfectNC_000017.11:g.663
36672_66336673ins5
4
GRCh38.p12First PassNC_000017.11Chr1766,336,67266,336,672
nssv16269535Submitted genomicNC_000017.10:g.643
32790_64332791ins5
4
GRCh37 (hg19)NC_000017.10Chr1764,332,79064,332,790

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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