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nsv5537970

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 30 studies. See in: genome view    
Submitted genomic165,029,619-165,029,632Question Mark
Overlapping variant regions from other studies: 162 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):164,747,407-164,747,420Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5537970Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3165,029,619165,029,632
nsv5537970RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3164,747,407164,747,420

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16942110insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16942110Submitted genomicNC_000003.12:g.165
029619_165029632in
s55
GRCh38 (hg38)NC_000003.12Chr3165,029,619165,029,632
nssv16942110RemappedPerfectNC_000003.11:g.164
747407_164747420in
s55
GRCh37.p13First PassNC_000003.11Chr3164,747,407164,747,420

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)
nssv169421100.004286404
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