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nsv5431302

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:66

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 278 SVs from 35 studies. See in: genome view    
Submitted genomic41,198,366-41,198,431Question Mark
Overlapping variant regions from other studies: 278 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):41,057,619-41,057,684Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5431302Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX41,198,36641,198,431
nsv5431302RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX41,057,61941,057,684

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17736550deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17736550Submitted genomicNC_000023.11:g.411
98366_41198431del
GRCh38 (hg38)NC_000023.11ChrX41,198,36641,198,431
nssv17736550RemappedPerfectNC_000023.10:g.410
57619_41057684del
GRCh37.p13First PassNC_000023.10ChrX41,057,61941,057,684

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)
nssv177365500.17811386394
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