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nsv5413798

  • 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: 114 SVs from 27 studies. See in: genome view    
Submitted genomic126,625,116-126,625,167Question Mark
Overlapping variant regions from other studies: 114 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):126,343,959-126,344,010Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5413798Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3126,625,116126,625,167
nsv5413798RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3126,343,959126,344,010

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16937648alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16937648Submitted genomicNC_000003.12:g.126
625116_126625167in
s278
GRCh38 (hg38)NC_000003.12Chr3126,625,116126,625,167
nssv16937648RemappedPerfectNC_000003.11:g.126
343959_126344010in
s278
GRCh37.p13First PassNC_000003.11Chr3126,343,959126,344,010

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)
nssv16937648<0.00116404
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