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nsv5561013

  • 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: 133 SVs from 30 studies. See in: genome view    
Submitted genomic55,970,136-55,970,187Question Mark
Overlapping variant regions from other studies: 133 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):56,882,695-56,882,746Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561013Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr855,970,13655,970,187
nsv5561013RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr856,882,69556,882,746

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17011706sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17011706Submitted genomicNC_000008.11:g.559
70136_55970187ins4
05
GRCh38 (hg38)NC_000008.11Chr855,970,13655,970,187
nssv17011706RemappedPerfectNC_000008.10:g.568
82695_56882746ins4
05
GRCh37.p13First PassNC_000008.10Chr856,882,69556,882,746

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)
nssv17011706<0.00116404
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