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nsv5414012

  • 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: 90 SVs from 23 studies. See in: genome view    
Submitted genomic14,047,029-14,047,080Question Mark
Overlapping variant regions from other studies: 90 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):13,950,346-13,950,397Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414012Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1714,047,02914,047,080
nsv5414012RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1713,950,34613,950,397

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17711596alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17711596Submitted genomicNC_000017.11:g.140
47029_14047080ins2
81
GRCh38 (hg38)NC_000017.11Chr1714,047,02914,047,080
nssv17711596RemappedPerfectNC_000017.10:g.139
50346_13950397ins2
81
GRCh37.p13First PassNC_000017.10Chr1713,950,34613,950,397

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)
nssv17711596<0.00116404
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