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nsv5411549

  • 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: 125 SVs from 24 studies. See in: genome view    
Submitted genomic212,332,716-212,332,767Question Mark
Overlapping variant regions from other studies: 129 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):212,506,058-212,506,109Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411549Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1212,332,716212,332,767
nsv5411549RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1212,506,058212,506,109

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16896095alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16896095Submitted genomicNC_000001.11:g.212
332716_212332767in
s280
GRCh38 (hg38)NC_000001.11Chr1212,332,716212,332,767
nssv16896095RemappedPerfectNC_000001.10:g.212
506058_212506109in
s280
GRCh37.p13First PassNC_000001.10Chr1212,506,058212,506,109

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)
nssv16896095<0.00116404
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