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nsv5437348

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,253

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 29 studies. See in: genome view    
Submitted genomic198,179,319-198,182,571Question Mark
Overlapping variant regions from other studies: 162 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):198,148,449-198,151,701Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5437348Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1198,179,319198,182,571
nsv5437348RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1198,148,449198,151,701

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894568deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894568Submitted genomicNC_000001.11:g.198
179319_198182571de
l
GRCh38 (hg38)NC_000001.11Chr1198,179,319198,182,571
nssv16894568RemappedPerfectNC_000001.10:g.198
148449_198151701de
l
GRCh37.p13First PassNC_000001.10Chr1198,148,449198,151,701

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)
nssv16894568<0.00116404
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