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nsv5516322

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:99

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 182 SVs from 28 studies. See in: genome view    
Submitted genomic82,248,092-82,248,190Question Mark
Overlapping variant regions from other studies: 182 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):80,205,968-80,206,066Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5516322Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1782,248,09282,248,190
nsv5516322RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1780,205,96880,206,066

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17715663duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17715663Submitted genomicNC_000017.11:g.822
48092_82248190dup
GRCh38 (hg38)NC_000017.11Chr1782,248,09282,248,190
nssv17715663RemappedPerfectNC_000017.10:g.802
05968_80206066dup
GRCh37.p13First PassNC_000017.10Chr1780,205,96880,206,066

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)
nssv17715663<0.00126404
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