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nsv5413878

  • 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: 135 SVs from 32 studies. See in: genome view    
Submitted genomic50,238,192-50,238,243Question Mark
Overlapping variant regions from other studies: 145 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):51,997,952-51,998,003Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5413878Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1050,238,19250,238,243
nsv5413878RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1051,997,95251,998,003

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17034683alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17034683Submitted genomicNC_000010.11:g.502
38192_50238243ins2
80
GRCh38 (hg38)NC_000010.11Chr1050,238,19250,238,243
nssv17034683RemappedPerfectNC_000010.10:g.519
97952_51998003ins2
80
GRCh37.p13First PassNC_000010.10Chr1051,997,95251,998,003

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)
nssv17034683<0.00116404
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