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nsv5546749

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:316,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2314 SVs from 105 studies. See in: genome view    
Submitted genomic21,955,564-22,271,564Question Mark
Overlapping variant regions from other studies: 2336 SVs from 105 studies. See in: genome view    
Remapped(Score: Good):22,309,936-22,625,947Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5546749Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2221,955,56422,271,564
nsv5546749RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2222,309,93622,625,947

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17727831duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17727831Submitted genomicNC_000022.11:g.219
55564_22271564dup
GRCh38 (hg38)NC_000022.11Chr2221,955,56422,271,564
nssv17727831RemappedGoodNC_000022.10:g.223
09936_22625947dup
GRCh37.p13First PassNC_000022.10Chr2222,309,93622,625,947

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)
nssv177278310.004276364
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