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nsv5419597

  • 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: 100 SVs from 16 studies. See in: genome view    
Submitted genomic68,875,182-68,875,233Question Mark
Overlapping variant regions from other studies: 100 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):66,871,323-66,871,374Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5419597Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1768,875,18268,875,233
nsv5419597RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1766,871,32366,871,374

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714239alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714239Submitted genomicNC_000017.11:g.688
75182_68875233ins2
80
GRCh38 (hg38)NC_000017.11Chr1768,875,18268,875,233
nssv17714239RemappedPerfectNC_000017.10:g.668
71323_66871374ins2
80
GRCh37.p13First PassNC_000017.10Chr1766,871,32366,871,374

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)
nssv17714239<0.00126404
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