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nsv5530211

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:111

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 14 studies. See in: genome view    
Submitted genomic58,092,343-58,092,453Question Mark
Overlapping variant regions from other studies: 107 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):56,169,704-56,169,814Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530211Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1758,092,34358,092,453
nsv5530211RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1756,169,70456,169,814

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713796duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713796Submitted genomicNC_000017.11:g.580
92343_58092453dup
GRCh38 (hg38)NC_000017.11Chr1758,092,34358,092,453
nssv17713796RemappedPerfectNC_000017.10:g.561
69704_56169814dup
GRCh37.p13First PassNC_000017.10Chr1756,169,70456,169,814

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)
nssv17713796<0.00116404
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