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nsv5549898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:191

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 19 studies. See in: genome view    
Submitted genomic41,216,115-41,216,305Question Mark
Overlapping variant regions from other studies: 162 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):42,588,042-42,588,232Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5549898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2141,216,11541,216,305
nsv5549898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2142,588,04242,588,232

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17726987deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17726987Submitted genomicNC_000021.9:g.4121
6115_41216305del
GRCh38 (hg38)NC_000021.9Chr2141,216,11541,216,305
nssv17726987RemappedPerfectNC_000021.8:g.4258
8042_42588232del
GRCh37.p13First PassNC_000021.8Chr2142,588,04242,588,232

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)
nssv17726987<0.00116404
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