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nsv5416846

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 255 SVs from 21 studies. See in: genome view    
Submitted genomic108,416,313-108,416,398Question Mark
Overlapping variant regions from other studies: 255 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):107,659,543-107,659,628Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5416846Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX108,416,313108,416,398
nsv5416846RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX107,659,543107,659,628

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741890deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741890Submitted genomicNC_000023.11:g.108
416313_108416398de
l
GRCh38 (hg38)NC_000023.11ChrX108,416,313108,416,398
nssv17741890RemappedPerfectNC_000023.10:g.107
659543_107659628de
l
GRCh37.p13First PassNC_000023.10ChrX107,659,543107,659,628

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)
nssv17741890<0.00116404
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