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nsv5414088

  • 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: 93 SVs from 16 studies. See in: genome view    
Submitted genomic61,599,753-61,599,804Question Mark
Overlapping variant regions from other studies: 93 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):61,891,952-61,892,003Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414088Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1561,599,75361,599,804
nsv5414088RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1561,891,95261,892,003

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17703214alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17703214Submitted genomicNC_000015.10:g.615
99753_61599804ins2
81
GRCh38 (hg38)NC_000015.10Chr1561,599,75361,599,804
nssv17703214RemappedPerfectNC_000015.9:g.6189
1952_61892003ins28
1
GRCh37.p13First PassNC_000015.9Chr1561,891,95261,892,003

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)
nssv17703214<0.00116404
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