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nsv5546011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 19 studies. See in: genome view    
Submitted genomic111,628,448-111,628,478Question Mark
Overlapping variant regions from other studies: 98 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):111,499,172-111,499,202Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5546011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11111,628,448111,628,478
nsv5546011RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11111,499,172111,499,202

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17050216insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17050216Submitted genomicNC_000011.10:g.111
628448_111628478in
s54
GRCh38 (hg38)NC_000011.10Chr11111,628,448111,628,478
nssv17050216RemappedPerfectNC_000011.9:g.1114
99172_111499202ins
54
GRCh37.p13First PassNC_000011.9Chr11111,499,172111,499,202

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)
nssv17050216<0.00166404
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