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nsv5411773

  • 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: 111 SVs from 24 studies. See in: genome view    
Submitted genomic146,545,009-146,545,060Question Mark
Overlapping variant regions from other studies: 111 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):146,262,796-146,262,847Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411773Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3146,545,009146,545,060
nsv5411773RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3146,262,796146,262,847

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16940455alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16940455Submitted genomicNC_000003.12:g.146
545009_146545060in
s279
GRCh38 (hg38)NC_000003.12Chr3146,545,009146,545,060
nssv16940455RemappedPerfectNC_000003.11:g.146
262796_146262847in
s279
GRCh37.p13First PassNC_000003.11Chr3146,262,796146,262,847

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)
nssv16940455<0.00116404
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