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nsv5530334

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 14 studies. See in: genome view    
Submitted genomic33,150,668-33,150,752Question Mark
Overlapping variant regions from other studies: 107 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):33,641,574-33,641,658Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530334Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1933,150,66833,150,752
nsv5530334RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1933,641,57433,641,658

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722860duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722860Submitted genomicNC_000019.10:g.331
50668_33150752dup
GRCh38 (hg38)NC_000019.10Chr1933,150,66833,150,752
nssv17722860RemappedPerfectNC_000019.9:g.3364
1574_33641658dup
GRCh37.p13First PassNC_000019.9Chr1933,641,57433,641,658

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)
nssv17722860<0.00116404
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