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nsv5904566

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:321

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 23 studies. See in: genome view    
Submitted genomic150,869,196-150,869,516Question Mark
Overlapping variant regions from other studies: 130 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):150,586,983-150,587,303Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5904566Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3150,869,196150,869,516
nsv5904566RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3150,586,983150,587,303

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17416220deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17416220Submitted genomicNC_000003.12:g.150
869196_150869516de
l
GRCh38 (hg38)NC_000003.12Chr3150,869,196150,869,516
nssv17416220RemappedPerfectNC_000003.11:g.150
586983_150587303de
l
GRCh37.p13First PassNC_000003.11Chr3150,586,983150,587,303

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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