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nsv5528734

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 67 SVs from 15 studies. See in: genome view    
Submitted genomic19,412,690-19,412,740Question Mark
Overlapping variant regions from other studies: 67 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):19,523,499-19,523,549Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528734Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1919,412,69019,412,740
nsv5528734RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1919,523,49919,523,549

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722104duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722104Submitted genomicNC_000019.10:g.194
12690_19412740dup
GRCh38 (hg38)NC_000019.10Chr1919,412,69019,412,740
nssv17722104RemappedPerfectNC_000019.9:g.1952
3499_19523549dup
GRCh37.p13First PassNC_000019.9Chr1919,523,49919,523,549

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)
nssv17722104<0.00116404
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