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nsv5418083

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,286

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 250 SVs from 19 studies. See in: genome view    
Submitted genomic129,456,232-129,459,517Question Mark
Overlapping variant regions from other studies: 250 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):128,590,209-128,593,494Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5418083Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX129,456,232129,459,517
nsv5418083RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX128,590,209128,593,494

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17737548duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17737548Submitted genomicNC_000023.11:g.129
456232_129459517du
p
GRCh38 (hg38)NC_000023.11ChrX129,456,232129,459,517
nssv17737548RemappedPerfectNC_000023.10:g.128
590209_128593494du
p
GRCh37.p13First PassNC_000023.10ChrX128,590,209128,593,494

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)
nssv17737548<0.00116404
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