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nsv5418740

  • 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: 96 SVs from 18 studies. See in: genome view    
Submitted genomic28,581,463-28,581,514Question Mark
Overlapping variant regions from other studies: 96 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):26,908,481-26,908,532Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5418740Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1728,581,46328,581,514
nsv5418740RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1726,908,48126,908,532

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712366alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712366Submitted genomicNC_000017.11:g.285
81463_28581514ins2
79
GRCh38 (hg38)NC_000017.11Chr1728,581,46328,581,514
nssv17712366RemappedPerfectNC_000017.10:g.269
08481_26908532ins2
79
GRCh37.p13First PassNC_000017.10Chr1726,908,48126,908,532

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)
nssv17712366<0.00116404
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