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nsv5419241

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
Submitted genomic48,159,019-48,159,070Question Mark
Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):48,451,216-48,451,267Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5419241Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1548,159,01948,159,070
nsv5419241RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1548,451,21648,451,267

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17701239alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17701239Submitted genomicNC_000015.10:g.481
59019_48159070ins2
81
GRCh38 (hg38)NC_000015.10Chr1548,159,01948,159,070
nssv17701239RemappedPerfectNC_000015.9:g.4845
1216_48451267ins28
1
GRCh37.p13First PassNC_000015.9Chr1548,451,21648,451,267

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)
nssv17701239<0.00126404
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