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nsv5426875

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,830

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 259 SVs from 21 studies. See in: genome view    
Submitted genomic110,099,050-110,100,879Question Mark
Overlapping variant regions from other studies: 259 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):109,342,278-109,344,107Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5426875Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX110,099,050110,100,879
nsv5426875RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX109,342,278109,344,107

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741947duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741947Submitted genomicNC_000023.11:g.110
099050_110100879du
p
GRCh38 (hg38)NC_000023.11ChrX110,099,050110,100,879
nssv17741947RemappedPerfectNC_000023.10:g.109
342278_109344107du
p
GRCh37.p13First PassNC_000023.10ChrX109,342,278109,344,107

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)
nssv17741947<0.00116404
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