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nsv5532143

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:391,160

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2141 SVs from 103 studies. See in: genome view    
Submitted genomic53,050,850-53,442,009Question Mark
Overlapping variant regions from other studies: 2141 SVs from 103 studies. See in: genome view    
Remapped(Score: Perfect):53,554,103-53,945,262Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5532143Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,050,85053,442,009
nsv5532143RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1953,554,10353,945,262

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724266duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724266Submitted genomicNC_000019.10:g.530
50850_53442009dup
GRCh38 (hg38)NC_000019.10Chr1953,050,85053,442,009
nssv17724266RemappedPerfectNC_000019.9:g.5355
4103_53945262dup
GRCh37.p13First PassNC_000019.9Chr1953,554,10353,945,262

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)
nssv17724266<0.00126404
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