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nsv5433283

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,583

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 377 SVs from 72 studies. See in: genome view    
Submitted genomic21,983,081-22,008,663Question Mark
Overlapping variant regions from other studies: 377 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):22,309,574-22,335,156Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5433283Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr121,983,08122,008,663
nsv5433283RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr122,309,57422,335,156

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902301duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902301Submitted genomicNC_000001.11:g.219
83081_22008663dup
GRCh38 (hg38)NC_000001.11Chr121,983,08122,008,663
nssv16902301RemappedPerfectNC_000001.10:g.223
09574_22335156dup
GRCh37.p13First PassNC_000001.10Chr122,309,57422,335,156

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)
nssv169023010.005296366
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