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nsv5518130

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,667

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 22 studies. See in: genome view    
Submitted genomic57,220,811-57,226,477Question Mark
Overlapping variant regions from other studies: 98 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):55,795,867-55,801,533Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518130Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2057,220,81157,226,477
nsv5518130RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2055,795,86755,801,533

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17733287deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17733287Submitted genomicNC_000020.11:g.572
20811_57226477del
GRCh38 (hg38)NC_000020.11Chr2057,220,81157,226,477
nssv17733287RemappedPerfectNC_000020.10:g.557
95867_55801533del
GRCh37.p13First PassNC_000020.10Chr2055,795,86755,801,533

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)
nssv17733287<0.00126404
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