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nsv5424055

  • 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: 117 SVs from 19 studies. See in: genome view    
Submitted genomic55,393,985-55,394,036Question Mark
Overlapping variant regions from other studies: 116 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):53,471,346-53,471,397Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424055Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1755,393,98555,394,036
nsv5424055RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1753,471,34653,471,397

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724765alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724765Submitted genomicNC_000017.11:g.553
93985_55394036ins2
81
GRCh38 (hg38)NC_000017.11Chr1755,393,98555,394,036
nssv17724765RemappedPerfectNC_000017.10:g.534
71346_53471397ins2
81
GRCh37.p13First PassNC_000017.10Chr1753,471,34653,471,397

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)
nssv17724765<0.00166404
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