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nsv5449581

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:332

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 25 studies. See in: genome view    
Submitted genomic221,512,988-221,513,319Question Mark
Overlapping variant regions from other studies: 125 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):222,377,708-222,378,039Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449581Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2221,512,988221,513,319
nsv5449581RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2222,377,708222,378,039

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928316deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928316Submitted genomicNC_000002.12:g.221
512988_221513319de
l
GRCh38 (hg38)NC_000002.12Chr2221,512,988221,513,319
nssv16928316RemappedPerfectNC_000002.11:g.222
377708_222378039de
l
GRCh37.p13First PassNC_000002.11Chr2222,377,708222,378,039

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)
nssv16928316<0.00126404
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