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nsv5400508

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 20 studies. See in: genome view    
Submitted genomic79,670,995-79,671,019Question Mark
Overlapping variant regions from other studies: 113 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):80,380,712-80,380,736Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400508Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr679,670,99579,671,019
nsv5400508RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr680,380,71280,380,736

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16983904alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16983904Submitted genomicNC_000006.12:g.796
70995_79671019ins2
81
GRCh38 (hg38)NC_000006.12Chr679,670,99579,671,019
nssv16983904RemappedPerfectNC_000006.11:g.803
80712_80380736ins2
81
GRCh37.p13First PassNC_000006.11Chr680,380,71280,380,736

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)
nssv16983904<0.00116404
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