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nsv5515415

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,505

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
Submitted genomic16,170,753-16,177,257Question Mark
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):16,281,564-16,288,068Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5515415Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1916,170,75316,177,257
nsv5515415RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1916,281,56416,288,068

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721842deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721842Submitted genomicNC_000019.10:g.161
70753_16177257del
GRCh38 (hg38)NC_000019.10Chr1916,170,75316,177,257
nssv17721842RemappedPerfectNC_000019.9:g.1628
1564_16288068del
GRCh37.p13First PassNC_000019.9Chr1916,281,56416,288,068

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)
nssv17721842<0.00116404
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