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nsv5544822

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 27 studies. See in: genome view    
Submitted genomic53,558,881-53,558,881Question Mark
Overlapping variant regions from other studies: 108 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):52,175,420-52,175,420Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5544822Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2053,558,88153,558,881
nsv5544822RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2052,175,42052,175,420

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17733050insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17733050Submitted genomicNC_000020.11:g.535
58881_53558882ins1
03
GRCh38 (hg38)NC_000020.11Chr2053,558,88153,558,881
nssv17733050RemappedPerfectNC_000020.10:g.521
75420_52175421ins1
03
GRCh37.p13First PassNC_000020.10Chr2052,175,42052,175,420

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)
nssv177330500.47425535388
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