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nsv5446038

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 20 studies. See in: genome view    
Submitted genomic207,123,354-207,123,406Question Mark
Overlapping variant regions from other studies: 129 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):207,296,699-207,296,751Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5446038Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1207,123,354207,123,406
nsv5446038RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1207,296,699207,296,751

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894974duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894974Submitted genomicNC_000001.11:g.207
123354_207123406du
p
GRCh38 (hg38)NC_000001.11Chr1207,123,354207,123,406
nssv16894974RemappedPerfectNC_000001.10:g.207
296699_207296751du
p
GRCh37.p13First PassNC_000001.10Chr1207,296,699207,296,751

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)
nssv16894974<0.00116404
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