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nsv5398512

  • 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: 76 SVs from 16 studies. See in: genome view    
Submitted genomic60,925,292-60,925,343Question Mark
Overlapping variant regions from other studies: 76 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):62,685,050-62,685,101Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5398512Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1060,925,29260,925,343
nsv5398512RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1062,685,05062,685,101

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17033890alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17033890Submitted genomicNC_000010.11:g.609
25292_60925343ins2
79
GRCh38 (hg38)NC_000010.11Chr1060,925,29260,925,343
nssv17033890RemappedPerfectNC_000010.10:g.626
85050_62685101ins2
79
GRCh37.p13First PassNC_000010.10Chr1062,685,05062,685,101

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)
nssv17033890<0.00116404
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