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nsv5516890

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,421

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 219 SVs from 39 studies. See in: genome view    
Submitted genomic20,033,614-20,041,034Question Mark
Overlapping variant regions from other studies: 190 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):20,144,423-20,151,843Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5516890Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1920,033,61420,041,034
nsv5516890RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1920,144,42320,151,843

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722159deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722159Submitted genomicNC_000019.10:g.200
33614_20041034del
GRCh38 (hg38)NC_000019.10Chr1920,033,61420,041,034
nssv17722159RemappedPerfectNC_000019.9:g.2014
4423_20151843del
GRCh37.p13First PassNC_000019.9Chr1920,144,42320,151,843

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)
nssv17722159<0.00116404
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