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nsv5404871

  • 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: 68 SVs from 23 studies. See in: genome view    
Submitted genomic59,209,109-59,209,160Question Mark
Overlapping variant regions from other studies: 68 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):58,976,582-58,976,633Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5404871Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1159,209,10959,209,160
nsv5404871RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1158,976,58258,976,633

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17045489alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17045489Submitted genomicNC_000011.10:g.592
09109_59209160ins2
80
GRCh38 (hg38)NC_000011.10Chr1159,209,10959,209,160
nssv17045489RemappedPerfectNC_000011.9:g.5897
6582_58976633ins28
0
GRCh37.p13First PassNC_000011.9Chr1158,976,58258,976,633

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)
nssv17045489<0.00116404
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