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nsv5445441

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 193 SVs from 41 studies. See in: genome view    
Submitted genomic155,780,712-155,780,797Question Mark
Overlapping variant regions from other studies: 193 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):155,498,501-155,498,586Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5445441Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3155,780,712155,780,797
nsv5445441RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3155,498,501155,498,586

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17734987deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17734987Submitted genomicNC_000003.12:g.155
780712_155780797de
l
GRCh38 (hg38)NC_000003.12Chr3155,780,712155,780,797
nssv17734987RemappedPerfectNC_000003.11:g.155
498501_155498586de
l
GRCh37.p13First PassNC_000003.11Chr3155,498,501155,498,586

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)
nssv17734987<0.00166404
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