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nsv5431534

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:82

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 289 SVs from 18 studies. See in: genome view    
Submitted genomic14,869,700-14,869,781Question Mark
Overlapping variant regions from other studies: 290 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):14,887,822-14,887,903Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5431534Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX14,869,70014,869,781
nsv5431534RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX14,887,82214,887,903

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739377deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739377Submitted genomicNC_000023.11:g.148
69700_14869781del
GRCh38 (hg38)NC_000023.11ChrX14,869,70014,869,781
nssv17739377RemappedPerfectNC_000023.10:g.148
87822_14887903del
GRCh37.p13First PassNC_000023.10ChrX14,887,82214,887,903

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)
nssv17739377<0.00116404
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