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nsv5395487

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 21 studies. See in: genome view    
Submitted genomic93,803,568-93,803,619Question Mark
Overlapping variant regions from other studies: 102 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):93,536,734-93,536,785Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5395487Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1193,803,56893,803,619
nsv5395487RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1193,536,73493,536,785

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052087alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052087Submitted genomicNC_000011.10:g.938
03568_93803619ins2
80
GRCh38 (hg38)NC_000011.10Chr1193,803,56893,803,619
nssv17052087RemappedPerfectNC_000011.9:g.9353
6734_93536785ins28
0
GRCh37.p13First PassNC_000011.9Chr1193,536,73493,536,785

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)
nssv17052087<0.00116404
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