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nsv5543886

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 298 SVs from 41 studies. See in: genome view    
Submitted genomic84,447,714-84,447,728Question Mark
Overlapping variant regions from other studies: 298 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):84,481,320-84,481,334Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5543886Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1684,447,71484,447,728
nsv5543886RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1684,481,32084,481,334

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17708314insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17708314Submitted genomicNC_000016.10:g.844
47714_84447728ins5
7
GRCh38 (hg38)NC_000016.10Chr1684,447,71484,447,728
nssv17708314RemappedPerfectNC_000016.9:g.8448
1320_84481334ins57
GRCh37.p13First PassNC_000016.9Chr1684,481,32084,481,334

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)
nssv177083140.0311966404
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