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nsv5502466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 23 studies. See in: genome view    
Submitted genomic40,800,473-40,800,537Question Mark
Overlapping variant regions from other studies: 136 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):41,374,609-41,374,673Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5502466Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1340,800,47340,800,537
nsv5502466RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1341,374,60941,374,673

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687110duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687110Submitted genomicNC_000013.11:g.408
00473_40800537dup
GRCh38 (hg38)NC_000013.11Chr1340,800,47340,800,537
nssv17687110RemappedPerfectNC_000013.10:g.413
74609_41374673dup
GRCh37.p13First PassNC_000013.10Chr1341,374,60941,374,673

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)
nssv17687110<0.00126404
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