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nsv4573120

  • 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: 398 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):20,761,759-20,761,759Question Mark
Overlapping variant regions from other studies: 398 SVs from 12 studies. See in: genome view    
Submitted genomic21,116,047-21,116,047Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573120RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2220,761,75920,761,759
nsv4573120Submitted genomicGRCh37.p13Primary AssemblyNC_000022.10Chr2221,116,04721,116,047

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16036510insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16036510RemappedPerfectNC_000022.11:g.207
61759_20761760ins6
4
GRCh38.p12First PassNC_000022.11Chr2220,761,75920,761,759
nssv16036510Submitted genomicNC_000022.10:g.211
16047_21116048ins6
4
GRCh37.p13NC_000022.10Chr2221,116,04721,116,047

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)
nssv16036510<0.001521614
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