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nsv5519767

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:84

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 20 studies. See in: genome view    
Submitted genomic44,519,196-44,519,279Question Mark
Overlapping variant regions from other studies: 130 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):43,147,837-43,147,920Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5519767Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2044,519,19644,519,279
nsv5519767RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2043,147,83743,147,920

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732552duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732552Submitted genomicNC_000020.11:g.445
19196_44519279dup
GRCh38 (hg38)NC_000020.11Chr2044,519,19644,519,279
nssv17732552RemappedPerfectNC_000020.10:g.431
47837_43147920dup
GRCh37.p13First PassNC_000020.10Chr2043,147,83743,147,920

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)
nssv17732552<0.00116404
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