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nsv6154241

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 17 studies. See in: genome view    
Submitted genomic136,187,246-136,187,325Question Mark
Overlapping variant regions from other studies: 103 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):135,906,088-135,906,167Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6154241Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3136,187,246136,187,325
nsv6154241RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3135,906,088135,906,167

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17861581deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17861581Submitted genomicNC_000003.12:g.136
187246_136187325de
l
GRCh38 (hg38)NC_000003.12Chr3136,187,246136,187,325
nssv17861581RemappedPerfectNC_000003.11:g.135
906088_135906167de
l
GRCh37.p13First PassNC_000003.11Chr3135,906,088135,906,167

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)
nssv17861581<0.00112340
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