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nsv5533712

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,261

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 141 SVs from 22 studies. See in: genome view    
Submitted genomic33,737,470-33,744,730Question Mark
Overlapping variant regions from other studies: 141 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):32,325,276-32,332,536Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533712Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2033,737,47033,744,730
nsv5533712RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2032,325,27632,332,536

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732045duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732045Submitted genomicNC_000020.11:g.337
37470_33744730dup
GRCh38 (hg38)NC_000020.11Chr2033,737,47033,744,730
nssv17732045RemappedPerfectNC_000020.10:g.323
25276_32332536dup
GRCh37.p13First PassNC_000020.10Chr2032,325,27632,332,536

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)
nssv17732045<0.00126404
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