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nsv5977315

  • 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: 166 SVs from 32 studies. See in: genome view    
Submitted genomic12,119,990-12,119,990Question Mark
Overlapping variant regions from other studies: 167 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):12,272,924-12,272,924Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5977315Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1212,119,99012,119,990
nsv5977315RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1212,272,92412,272,924

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17363420insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17363420Submitted genomicNC_000012.12:g.121
19990_12119991ins1
55
GRCh38 (hg38)NC_000012.12Chr1212,119,99012,119,990
nssv17363420RemappedPerfectNC_000012.11:g.122
72924_12272925ins1
55
GRCh37.p13First PassNC_000012.11Chr1212,272,92412,272,924

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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