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nsv5522044

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 21 studies. See in: genome view    
Submitted genomic56,451,021-56,451,074Question Mark
Overlapping variant regions from other studies: 109 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):56,962,390-56,962,443Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5522044Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1956,451,02156,451,074
nsv5522044RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1956,962,39056,962,443

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725789duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725789Submitted genomicNC_000019.10:g.564
51021_56451074dup
GRCh38 (hg38)NC_000019.10Chr1956,451,02156,451,074
nssv17725789RemappedPerfectNC_000019.9:g.5696
2390_56962443dup
GRCh37.p13First PassNC_000019.9Chr1956,962,39056,962,443

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)
nssv17725789<0.00116404
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