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nsv5415960

  • 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: 171 SVs from 15 studies. See in: genome view    
Submitted genomic54,299,612-54,299,663Question Mark
Overlapping variant regions from other studies: 171 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):51,825,982-51,826,033Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5415960Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1854,299,61254,299,663
nsv5415960RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1851,825,98251,826,033

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17718318alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17718318Submitted genomicNC_000018.10:g.542
99612_54299663ins2
81
GRCh38 (hg38)NC_000018.10Chr1854,299,61254,299,663
nssv17718318RemappedPerfectNC_000018.9:g.5182
5982_51826033ins28
1
GRCh37.p13First PassNC_000018.9Chr1851,825,98251,826,033

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)
nssv17718318<0.00126404
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