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nsv5559017

  • 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: 449 SVs from 58 studies. See in: genome view    
Submitted genomic45,583,245-45,583,296Question Mark
Overlapping variant regions from other studies: 447 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):43,660,611-43,660,662Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559017Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1745,583,24545,583,296
nsv5559017RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1743,660,61143,660,662

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713388sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713388Submitted genomicNC_000017.11:g.455
83245_45583296ins1
304
GRCh38 (hg38)NC_000017.11Chr1745,583,24545,583,296
nssv17713388RemappedPerfectNC_000017.10:g.436
60611_43660662ins1
304
GRCh37.p13First PassNC_000017.10Chr1743,660,61143,660,662

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)
nssv177133880.0644046284
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