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nsv5397589

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 17 studies. See in: genome view    
Submitted genomic182,921,780-182,921,831Question Mark
Overlapping variant regions from other studies: 83 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):182,639,568-182,639,619Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5397589Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3182,921,780182,921,831
nsv5397589RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3182,639,568182,639,619

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16942549alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16942549Submitted genomicNC_000003.12:g.182
921780_182921831in
s279
GRCh38 (hg38)NC_000003.12Chr3182,921,780182,921,831
nssv16942549RemappedPerfectNC_000003.11:g.182
639568_182639619in
s279
GRCh37.p13First PassNC_000003.11Chr3182,639,568182,639,619

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)
nssv16942549<0.00116404
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