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nsv5428791

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,215

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 397 SVs from 22 studies. See in: genome view    
Submitted genomic3,103,499-3,104,713Question Mark
Overlapping variant regions from other studies: 398 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):3,021,540-3,022,754Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5428791Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX3,103,4993,104,713
nsv5428791RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX3,021,5403,022,754

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17736096deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17736096Submitted genomicNC_000023.11:g.310
3499_3104713del
GRCh38 (hg38)NC_000023.11ChrX3,103,4993,104,713
nssv17736096RemappedPerfectNC_000023.10:g.302
1540_3022754del
GRCh37.p13First PassNC_000023.10ChrX3,021,5403,022,754

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)
nssv17736096<0.00116404
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