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nsv5895943

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:506

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 233 SVs from 44 studies. See in: genome view    
Submitted genomic197,824,351-197,824,856Question Mark
Overlapping variant regions from other studies: 233 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):197,551,222-197,551,727Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5895943Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3197,824,351197,824,856
nsv5895943RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3197,551,222197,551,727

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17428824duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17428824Submitted genomicNC_000003.12:g.197
824351_197824856du
p
GRCh38 (hg38)NC_000003.12Chr3197,824,351197,824,856
nssv17428824RemappedPerfectNC_000003.11:g.197
551222_197551727du
p
GRCh37.p13First PassNC_000003.11Chr3197,551,222197,551,727

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)
nssv17428824<0.0011764
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