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nsv5508118

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:929

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
Submitted genomic111,692,192-111,693,120Question Mark
Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):111,562,916-111,563,844Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5508118Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11111,692,192111,693,120
nsv5508118RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11111,562,916111,563,844

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17688436deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17688436Submitted genomicNC_000011.10:g.111
692192_111693120de
l
GRCh38 (hg38)NC_000011.10Chr11111,692,192111,693,120
nssv17688436RemappedPerfectNC_000011.9:g.1115
62916_111563844del
GRCh37.p13First PassNC_000011.9Chr11111,562,916111,563,844

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)
nssv17688436<0.00166404
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