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nsv5493969

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,675

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 466 SVs from 51 studies. See in: genome view    
Submitted genomic114,587,124-114,632,798Question Mark
Overlapping variant regions from other studies: 466 SVs from 51 studies. See in: genome view    
Remapped(Score: Perfect):114,457,846-114,503,520Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5493969Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11114,587,124114,632,798
nsv5493969RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11114,457,846114,503,520

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052564deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052564Submitted genomicNC_000011.10:g.114
587124_114632798de
l
GRCh38 (hg38)NC_000011.10Chr11114,587,124114,632,798
nssv17052564RemappedPerfectNC_000011.9:g.1144
57846_114503520del
GRCh37.p13First PassNC_000011.9Chr11114,457,846114,503,520

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)
nssv17052564<0.00116404
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