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nsv5441885

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:882

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 272 SVs from 49 studies. See in: genome view    
Submitted genomic196,329,087-196,329,968Question Mark
Overlapping variant regions from other studies: 272 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):196,055,958-196,056,839Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5441885Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3196,329,087196,329,968
nsv5441885RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3196,055,958196,056,839

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16944621deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16944621Submitted genomicNC_000003.12:g.196
329087_196329968de
l
GRCh38 (hg38)NC_000003.12Chr3196,329,087196,329,968
nssv16944621RemappedPerfectNC_000003.11:g.196
055958_196056839de
l
GRCh37.p13First PassNC_000003.11Chr3196,055,958196,056,839

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)
nssv169446210.37423946404
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