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nsv5429150

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,259

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 250 SVs from 27 studies. See in: genome view    
Submitted genomic54,956,523-54,957,781Question Mark
Overlapping variant regions from other studies: 244 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):54,982,956-54,984,214Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5429150Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX54,956,52354,957,781
nsv5429150RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX54,982,95654,984,214

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740180deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740180Submitted genomicNC_000023.11:g.549
56523_54957781del
GRCh38 (hg38)NC_000023.11ChrX54,956,52354,957,781
nssv17740180RemappedPerfectNC_000023.10:g.549
82956_54984214del
GRCh37.p13First PassNC_000023.10ChrX54,982,95654,984,214

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)
nssv17740180<0.00146404
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