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nsv5540196

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 29 studies. See in: genome view    
Submitted genomic114,577,056-114,577,062Question Mark
Overlapping variant regions from other studies: 106 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):114,447,778-114,447,784Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5540196Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11114,577,056114,577,062
nsv5540196RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11114,447,778114,447,784

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17688437insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17688437Submitted genomicNC_000011.10:g.114
577056_114577062in
s108
GRCh38 (hg38)NC_000011.10Chr11114,577,056114,577,062
nssv17688437RemappedPerfectNC_000011.9:g.1144
47778_114447784ins
108
GRCh37.p13First PassNC_000011.9Chr11114,447,778114,447,784

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)
nssv17688437<0.00116404
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