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nsv5506004

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:932

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 31 studies. See in: genome view    
Submitted genomic12,253,055-12,253,986Question Mark
Overlapping variant regions from other studies: 145 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):12,405,989-12,406,920Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5506004Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1212,253,05512,253,986
nsv5506004RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1212,405,98912,406,920

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17055939duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17055939Submitted genomicNC_000012.12:g.122
53055_12253986dup
GRCh38 (hg38)NC_000012.12Chr1212,253,05512,253,986
nssv17055939RemappedPerfectNC_000012.11:g.124
05989_12406920dup
GRCh37.p13First PassNC_000012.11Chr1212,405,98912,406,920

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)
nssv170559390.003176404
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