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nsv5405107

  • 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: 117 SVs from 21 studies. See in: genome view    
Submitted genomic53,820,199-53,820,250Question Mark
Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):54,047,336-54,047,387Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5405107Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr253,820,19953,820,250
nsv5405107RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr254,047,33654,047,387

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16913095alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16913095Submitted genomicNC_000002.12:g.538
20199_53820250ins2
81
GRCh38 (hg38)NC_000002.12Chr253,820,19953,820,250
nssv16913095RemappedPerfectNC_000002.11:g.540
47336_54047387ins2
81
GRCh37.p13First PassNC_000002.11Chr254,047,33654,047,387

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)
nssv16913095<0.00116404
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