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nsv4578230

  • 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: 32 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):17,518,955-17,518,955Question Mark
Overlapping variant regions from other studies: 32 SVs from 7 studies. See in: genome view    
Submitted genomic17,629,764-17,629,764Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578230RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1917,518,95517,518,955
nsv4578230Submitted genomicGRCh37.p13Primary AssemblyNC_000019.9Chr1917,629,76417,629,764

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16022654sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16022654RemappedPerfectNC_000019.10:g.175
18955_17518956ins1
239
GRCh38.p12First PassNC_000019.10Chr1917,518,95517,518,955
nssv16022654Submitted genomicNC_000019.9:g.1762
9764_17629765ins12
39
GRCh37.p13NC_000019.9Chr1917,629,76417,629,764

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)
nssv160226544.6e-005121694
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