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nsv5557417

  • 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: 73 SVs from 19 studies. See in: genome view    
Submitted genomic43,054,424-43,054,475Question Mark
Overlapping variant regions from other studies: 73 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):43,095,916-43,095,967Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5557417Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr343,054,42443,054,475
nsv5557417RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr343,095,91643,095,967

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16931950sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16931950Submitted genomicNC_000003.12:g.430
54424_43054475ins1
240
GRCh38 (hg38)NC_000003.12Chr343,054,42443,054,475
nssv16931950RemappedPerfectNC_000003.11:g.430
95916_43095967ins1
240
GRCh37.p13First PassNC_000003.11Chr343,095,91643,095,967

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)
nssv16931950<0.00116404
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