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nsv5559443

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 134 SVs from 35 studies. See in: genome view    
Submitted genomic87,053,491-87,053,569Question Mark
Overlapping variant regions from other studies: 134 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):87,280,614-87,280,692Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559443Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr287,053,49187,053,569
nsv5559443RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr287,280,61487,280,692

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16916673sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16916673Submitted genomicNC_000002.12:g.870
53491_87053569ins3
46
GRCh38 (hg38)NC_000002.12Chr287,053,49187,053,569
nssv16916673RemappedPerfectNC_000002.11:g.872
80614_87280692ins3
46
GRCh37.p13First PassNC_000002.11Chr287,280,61487,280,692

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)
nssv16916673<0.00116404
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