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nsv5423374

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 256 SVs from 20 studies. See in: genome view    
Submitted genomic106,914,987-106,915,057Question Mark
Overlapping variant regions from other studies: 256 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):106,158,217-106,158,287Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423374Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX106,914,987106,915,057
nsv5423374RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX106,158,217106,158,287

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741848duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741848Submitted genomicNC_000023.11:g.106
914987_106915057du
p
GRCh38 (hg38)NC_000023.11ChrX106,914,987106,915,057
nssv17741848RemappedPerfectNC_000023.10:g.106
158217_106158287du
p
GRCh37.p13First PassNC_000023.10ChrX106,158,217106,158,287

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)
nssv17741848<0.00136400
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