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nsv5420568

  • 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: 66 SVs from 21 studies. See in: genome view    
Submitted genomic21,663,036-21,663,087Question Mark
Overlapping variant regions from other studies: 66 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):22,131,249-22,131,300Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5420568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1421,663,03621,663,087
nsv5420568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1422,131,24922,131,300

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17695351alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17695351Submitted genomicNC_000014.9:g.2166
3036_21663087ins27
8
GRCh38 (hg38)NC_000014.9Chr1421,663,03621,663,087
nssv17695351RemappedPerfectNC_000014.8:g.2213
1249_22131300ins27
8
GRCh37.p13First PassNC_000014.8Chr1422,131,24922,131,300

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)
nssv17695351<0.00116404
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