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nsv5550225

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 183 SVs from 27 studies. See in: genome view    
Submitted genomic36,008,572-36,008,587Question Mark
Overlapping variant regions from other studies: 183 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):33,588,535-33,588,550Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5550225Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1836,008,57236,008,587
nsv5550225RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1833,588,53533,588,550

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17717343insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17717343Submitted genomicNC_000018.10:g.360
08572_36008587ins5
6
GRCh38 (hg38)NC_000018.10Chr1836,008,57236,008,587
nssv17717343RemappedPerfectNC_000018.9:g.3358
8535_33588550ins56
GRCh37.p13First PassNC_000018.9Chr1833,588,53533,588,550

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)
nssv177173430.014896376
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