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nsv5465847

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,165

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 122 SVs from 24 studies. See in: genome view    
Submitted genomic122,642,174-122,643,338Question Mark
Overlapping variant regions from other studies: 122 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):123,563,329-123,564,493Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5465847Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4122,642,174122,643,338
nsv5465847RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4123,563,329123,564,493

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16955199deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16955199Submitted genomicNC_000004.12:g.122
642174_122643338de
l
GRCh38 (hg38)NC_000004.12Chr4122,642,174122,643,338
nssv16955199RemappedPerfectNC_000004.11:g.123
563329_123564493de
l
GRCh37.p13First PassNC_000004.11Chr4123,563,329123,564,493

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)
nssv16955199<0.00116404
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