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nsv4578234

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 26 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):42,445,074-42,445,074Question Mark
Overlapping variant regions from other studies: 26 SVs from 4 studies. See in: genome view    
Submitted genomic42,737,272-42,737,272Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578234RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1542,445,07442,445,074
nsv4578234Submitted genomicGRCh37.p13Primary AssemblyNC_000015.9Chr1542,737,27242,737,272

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16012317sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16012317RemappedPerfectNC_000015.10:g.424
45074_42445075ins1
236
GRCh38.p12First PassNC_000015.10Chr1542,445,07442,445,074
nssv16012317Submitted genomicNC_000015.9:g.4273
7272_42737273ins12
36
GRCh37.p13NC_000015.9Chr1542,737,27242,737,272

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)
nssv160123174.6e-005121694
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