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nsv5518398

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,368

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 149 SVs from 31 studies. See in: genome view    
Submitted genomic40,447,657-40,453,024Question Mark
Overlapping variant regions from other studies: 149 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):40,953,564-40,958,931Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518398Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1940,447,65740,453,024
nsv5518398RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1940,953,56440,958,931

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723407deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723407Submitted genomicNC_000019.10:g.404
47657_40453024del
GRCh38 (hg38)NC_000019.10Chr1940,447,65740,453,024
nssv17723407RemappedPerfectNC_000019.9:g.4095
3564_40958931del
GRCh37.p13First PassNC_000019.9Chr1940,953,56440,958,931

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17723407<0.00116404
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