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nsv5546920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,287

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 239 SVs from 48 studies. See in: genome view    
Submitted genomic39,031,269-39,048,555Question Mark
Overlapping variant regions from other studies: 239 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):39,427,274-39,444,560Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5546920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2239,031,26939,048,555
nsv5546920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2239,427,27439,444,560

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17728978duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17728978Submitted genomicNC_000022.11:g.390
31269_39048555dup
GRCh38 (hg38)NC_000022.11Chr2239,031,26939,048,555
nssv17728978RemappedPerfectNC_000022.10:g.394
27274_39444560dup
GRCh37.p13First PassNC_000022.10Chr2239,427,27439,444,560

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)
nssv177289780.004266400
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