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nsv5424731

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:221

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 284 SVs from 19 studies. See in: genome view    
Submitted genomic14,775,889-14,776,109Question Mark
Overlapping variant regions from other studies: 285 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):14,794,011-14,794,231Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424731Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX14,775,88914,776,109
nsv5424731RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX14,794,01114,794,231

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739373deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739373Submitted genomicNC_000023.11:g.147
75889_14776109del
GRCh38 (hg38)NC_000023.11ChrX14,775,88914,776,109
nssv17739373RemappedPerfectNC_000023.10:g.147
94011_14794231del
GRCh37.p13First PassNC_000023.10ChrX14,794,01114,794,231

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)
nssv17739373<0.00166404
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