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nsv5526823

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:931

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 24 studies. See in: genome view    
Submitted genomic44,989,836-44,990,766Question Mark
Overlapping variant regions from other studies: 119 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):43,618,477-43,619,407Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526823Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2044,989,83644,990,766
nsv5526823RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2043,618,47743,619,407

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732589deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732589Submitted genomicNC_000020.11:g.449
89836_44990766del
GRCh38 (hg38)NC_000020.11Chr2044,989,83644,990,766
nssv17732589RemappedPerfectNC_000020.10:g.436
18477_43619407del
GRCh37.p13First PassNC_000020.10Chr2043,618,47743,619,407

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)
nssv17732589<0.00126404
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