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nsv5560614

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 310 SVs from 27 studies. See in: genome view    
Submitted genomic18,260,594-18,260,646Question Mark
Overlapping variant regions from other studies: 311 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):18,278,714-18,278,766Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5560614Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX18,260,59418,260,646
nsv5560614RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX18,278,71418,278,766

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739486alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739486Submitted genomicNC_000023.11:g.182
60594_18260646ins2
68
GRCh38 (hg38)NC_000023.11ChrX18,260,59418,260,646
nssv17739486RemappedPerfectNC_000023.10:g.182
78714_18278766ins2
68
GRCh37.p13First PassNC_000023.10ChrX18,278,71418,278,766

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)
nssv177394860.0231506404
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