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nsv5565459

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,032

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 255 SVs from 43 studies. See in: genome view    
Submitted genomic37,448,355-37,451,386Question Mark
Overlapping variant regions from other studies: 255 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):37,448,457-37,451,488Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5565459Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr537,448,35537,451,386
nsv5565459RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr537,448,45737,451,488

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17126031deletionHG03732SequencingSequence alignment1,582

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17126031Submitted genomicNC_000005.10:g.374
48355_37451386delC
GRCh38 (hg38)NC_000005.10Chr537,448,35537,451,386
nssv17126031RemappedPerfectNC_000005.9:g.3744
8457_37451488delC
GRCh37.p13First PassNC_000005.9Chr537,448,45737,451,488

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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