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nsv4754592

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:190,072,072

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 557825 SVs from 161 studies. See in: genome view    
Remapped(Score: Good):27,111-190,099,182Question Mark
Overlapping variant regions from other studies: 557516 SVs from 161 studies. See in: genome view    
Submitted genomic27,111-191,020,337Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4754592RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr427,111190,099,182
nsv4754592Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr427,111191,020,337

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16289974inversionSequencingSplit read mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16289974RemappedGoodNC_000004.12:g.271
11_190099182inv
GRCh38.p12First PassNC_000004.12Chr427,111190,099,182
nssv16289974Submitted genomicNC_000004.11:g.271
11_191020337inv
GRCh37 (hg19)NC_000004.11Chr427,111191,020,337

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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