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nsv5524155

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:262

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 175 SVs from 16 studies. See in: genome view    
Submitted genomic49,825,928-49,826,189Question Mark
Overlapping variant regions from other studies: 175 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):47,352,298-47,352,559Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5524155Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1849,825,92849,826,189
nsv5524155RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1847,352,29847,352,559

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17718087deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17718087Submitted genomicNC_000018.10:g.498
25928_49826189del
GRCh38 (hg38)NC_000018.10Chr1849,825,92849,826,189
nssv17718087RemappedPerfectNC_000018.9:g.4735
2298_47352559del
GRCh37.p13First PassNC_000018.9Chr1847,352,29847,352,559

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)
nssv17718087<0.00136404
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