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nsv5518169

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,667

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 31 studies. See in: genome view    
Submitted genomic48,912,326-48,913,992Question Mark
Overlapping variant regions from other studies: 98 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):49,415,583-49,417,249Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518169Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,912,32648,913,992
nsv5518169RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,415,58349,417,249

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723933deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723933Submitted genomicNC_000019.10:g.489
12326_48913992del
GRCh38 (hg38)NC_000019.10Chr1948,912,32648,913,992
nssv17723933RemappedPerfectNC_000019.9:g.4941
5583_49417249del
GRCh37.p13First PassNC_000019.9Chr1949,415,58349,417,249

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)
nssv17723933<0.00116404
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