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nsv5908212

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,443

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 172 SVs from 34 studies. See in: genome view    
Submitted genomic12,234,085-12,235,527Question Mark
Overlapping variant regions from other studies: 173 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):12,387,019-12,388,461Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5908212Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1212,234,08512,235,527
nsv5908212RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1212,387,01912,388,461

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17369090deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17369090Submitted genomicNC_000012.12:g.122
34085_12235527del
GRCh38 (hg38)NC_000012.12Chr1212,234,08512,235,527
nssv17369090RemappedPerfectNC_000012.11:g.123
87019_12388461del
GRCh37.p13First PassNC_000012.11Chr1212,387,01912,388,461

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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