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nsv5400217

  • 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: 90 SVs from 20 studies. See in: genome view    
Submitted genomic231,118,124-231,118,124Question Mark
Overlapping variant regions from other studies: 90 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):231,982,838-231,982,838Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400217Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2231,118,124231,118,124
nsv5400217RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2231,982,838231,982,838

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928551alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928551Submitted genomicNC_000002.12:g.231
118124_231118125in
s285
GRCh38 (hg38)NC_000002.12Chr2231,118,124231,118,124
nssv16928551RemappedPerfectNC_000002.11:g.231
982838_231982839in
s285
GRCh37.p13First PassNC_000002.11Chr2231,982,838231,982,838

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)
nssv169285510.0281816384
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