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nsv5933537

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:833

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 35 studies. See in: genome view    
Submitted genomic123,353,393-123,354,225Question Mark
Overlapping variant regions from other studies: 146 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):123,837,940-123,838,772Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5933537Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12123,353,393123,354,225
nsv5933537RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12123,837,940123,838,772

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17355775deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17355775Submitted genomicNC_000012.12:g.123
353393_123354225de
l
GRCh38 (hg38)NC_000012.12Chr12123,353,393123,354,225
nssv17355775RemappedPerfectNC_000012.11:g.123
837940_123838772de
l
GRCh37.p13First PassNC_000012.11Chr12123,837,940123,838,772

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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