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nsv5433495

  • 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: 108 SVs from 12 studies. See in: genome view    
Submitted genomic77,990,646-77,990,697Question Mark
Overlapping variant regions from other studies: 108 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):75,986,727-75,986,778Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5433495Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1777,990,64677,990,697
nsv5433495RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1775,986,72775,986,778

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714818alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714818Submitted genomicNC_000017.11:g.779
90646_77990697ins2
80
GRCh38 (hg38)NC_000017.11Chr1777,990,64677,990,697
nssv17714818RemappedPerfectNC_000017.10:g.759
86727_75986778ins2
80
GRCh37.p13First PassNC_000017.10Chr1775,986,72775,986,778

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)
nssv17714818<0.00116404
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