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nsv5530898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 17 studies. See in: genome view    
Submitted genomic40,132,334-40,132,388Question Mark
Overlapping variant regions from other studies: 119 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):38,288,587-38,288,641Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1740,132,33440,132,388
nsv5530898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1738,288,58738,288,641

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713078deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713078Submitted genomicNC_000017.11:g.401
32334_40132388del
GRCh38 (hg38)NC_000017.11Chr1740,132,33440,132,388
nssv17713078RemappedPerfectNC_000017.10:g.382
88587_38288641del
GRCh37.p13First PassNC_000017.10Chr1738,288,58738,288,641

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)
nssv17713078<0.00116404
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