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nsv5505186

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:160,585

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 476 SVs from 60 studies. See in: genome view    
Submitted genomic10,720,422-10,881,006Question Mark
Overlapping variant regions from other studies: 477 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):10,873,021-11,033,605Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5505186Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1210,720,42210,881,006
nsv5505186RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,873,02111,033,605

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053057duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053057Submitted genomicNC_000012.12:g.107
20422_10881006dup
GRCh38 (hg38)NC_000012.12Chr1210,720,42210,881,006
nssv17053057RemappedPerfectNC_000012.11:g.108
73021_11033605dup
GRCh37.p13First PassNC_000012.11Chr1210,873,02111,033,605

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)
nssv17053057<0.00146404
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