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nsv5515730

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,213

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 30 studies. See in: genome view    
Submitted genomic15,389,548-15,395,760Question Mark
Overlapping variant regions from other studies: 124 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):15,500,359-15,506,571Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5515730Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1915,389,54815,395,760
nsv5515730RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1915,500,35915,506,571

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721765duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721765Submitted genomicNC_000019.10:g.153
89548_15395760dup
GRCh38 (hg38)NC_000019.10Chr1915,389,54815,395,760
nssv17721765RemappedPerfectNC_000019.9:g.1550
0359_15506571dup
GRCh37.p13First PassNC_000019.9Chr1915,500,35915,506,571

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)
nssv17721765<0.00116404
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