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nsv5520420

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:358

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 178 SVs from 32 studies. See in: genome view    
Submitted genomic20,036,575-20,036,932Question Mark
Overlapping variant regions from other studies: 150 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):20,147,384-20,147,741Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5520420Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1920,036,57520,036,932
nsv5520420RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1920,147,38420,147,741

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722160duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722160Submitted genomicNC_000019.10:g.200
36575_20036932dup
GRCh38 (hg38)NC_000019.10Chr1920,036,57520,036,932
nssv17722160RemappedPerfectNC_000019.9:g.2014
7384_20147741dup
GRCh37.p13First PassNC_000019.9Chr1920,147,38420,147,741

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)
nssv17722160<0.00146404
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