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nsv5514204

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:144

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 189 SVs from 31 studies. See in: genome view    
Submitted genomic15,842,207-15,842,350Question Mark
Overlapping variant regions from other studies: 189 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):17,214,526-17,214,669Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514204Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2115,842,20715,842,350
nsv5514204RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2117,214,52617,214,669

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17734117deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17734117Submitted genomicNC_000021.9:g.1584
2207_15842350del
GRCh38 (hg38)NC_000021.9Chr2115,842,20715,842,350
nssv17734117RemappedPerfectNC_000021.8:g.1721
4526_17214669del
GRCh37.p13First PassNC_000021.8Chr2117,214,52617,214,669

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)
nssv17734117<0.00126404
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