nsv5950031

  • 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: 165 SVs from 31 studies. See in: genome view    
Submitted genomic140,362,274-140,362,274Question Mark
Overlapping variant regions from other studies: 165 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):141,283,428-141,283,428Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5950031Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4140,362,274140,362,274
nsv5950031RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4141,283,428141,283,428

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17423502insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17423502Submitted genomicNC_000004.12:g.140
362274_140362275in
s66
GRCh38 (hg38)NC_000004.12Chr4140,362,274140,362,274
nssv17423502RemappedPerfectNC_000004.11:g.141
283428_141283429in
s66
GRCh37.p13First PassNC_000004.11Chr4141,283,428141,283,428

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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