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nsv5518313

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:619

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 26 studies. See in: genome view    
Submitted genomic3,686,667-3,687,285Question Mark
Overlapping variant regions from other studies: 130 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):3,667,314-3,667,932Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518313Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr203,686,6673,687,285
nsv5518313RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr203,667,3143,667,932

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17730428deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17730428Submitted genomicNC_000020.11:g.368
6667_3687285del
GRCh38 (hg38)NC_000020.11Chr203,686,6673,687,285
nssv17730428RemappedPerfectNC_000020.10:g.366
7314_3667932del
GRCh37.p13First PassNC_000020.10Chr203,667,3143,667,932

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)
nssv17730428<0.00126404
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