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nsv5518166

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,393

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 30 studies. See in: genome view    
Submitted genomic15,388,592-15,395,984Question Mark
Overlapping variant regions from other studies: 128 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):15,499,403-15,506,795Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518166Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1915,388,59215,395,984
nsv5518166RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1915,499,40315,506,795

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721764deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721764Submitted genomicNC_000019.10:g.153
88592_15395984del
GRCh38 (hg38)NC_000019.10Chr1915,388,59215,395,984
nssv17721764RemappedPerfectNC_000019.9:g.1549
9403_15506795del
GRCh37.p13First PassNC_000019.9Chr1915,499,40315,506,795

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)
nssv17721764<0.00146404
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