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nsv5948749

  • 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: 188 SVs from 33 studies. See in: genome view    
Submitted genomic15,379,415-15,379,415Question Mark
Overlapping variant regions from other studies: 188 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):15,519,539-15,519,539Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5948749Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr215,379,41515,379,415
nsv5948749RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr215,519,53915,519,539

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17391074insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17391074Submitted genomicNC_000002.12:g.153
79415_15379416ins3
12
GRCh38 (hg38)NC_000002.12Chr215,379,41515,379,415
nssv17391074RemappedPerfectNC_000002.11:g.155
19539_15519540ins3
12
GRCh37.p13First PassNC_000002.11Chr215,519,53915,519,539

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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