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nsv5506157

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,065

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 16 studies. See in: genome view    
Submitted genomic113,799,418-113,801,482Question Mark
Overlapping variant regions from other studies: 97 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):113,670,140-113,672,204Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5506157Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11113,799,418113,801,482
nsv5506157RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11113,670,140113,672,204

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052471deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052471Submitted genomicNC_000011.10:g.113
799418_113801482de
l
GRCh38 (hg38)NC_000011.10Chr11113,799,418113,801,482
nssv17052471RemappedPerfectNC_000011.9:g.1136
70140_113672204del
GRCh37.p13First PassNC_000011.9Chr11113,670,140113,672,204

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)
nssv170524710.005316400
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