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nsv5400369

  • 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: 98 SVs from 17 studies. See in: genome view    
Submitted genomic213,085,453-213,085,453Question Mark
Overlapping variant regions from other studies: 98 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):213,950,177-213,950,177Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400369Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2213,085,453213,085,453
nsv5400369RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2213,950,177213,950,177

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16923747alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16923747Submitted genomicNC_000002.12:g.213
085453_213085454in
s317
GRCh38 (hg38)NC_000002.12Chr2213,085,453213,085,453
nssv16923747RemappedPerfectNC_000002.11:g.213
950177_213950178in
s317
GRCh37.p13First PassNC_000002.11Chr2213,950,177213,950,177

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)
nssv16923747<0.00136404
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