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nsv5614301

  • 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: 128 SVs from 29 studies. See in: genome view    
Submitted genomic55,873,983-55,873,983Question Mark
Overlapping variant regions from other studies: 128 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):56,101,118-56,101,118Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5614301Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr255,873,98355,873,983
nsv5614301RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr256,101,11856,101,118

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17113345insertionSAMN00000485SequencingSequence alignment1,404

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17113345Submitted genomicNC_000002.12:g.558
73983_55873984ins3
47
GRCh38 (hg38)NC_000002.12Chr255,873,98355,873,983
nssv17113345RemappedPerfectNC_000002.11:g.561
01118_56101119ins3
47
GRCh37.p13First PassNC_000002.11Chr256,101,11856,101,118

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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