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nsv5421206

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:99

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 172 SVs from 37 studies. See in: genome view    
Submitted genomic21,766,241-21,766,339Question Mark
Overlapping variant regions from other studies: 172 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):21,949,043-21,949,141Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5421206Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1921,766,24121,766,339
nsv5421206RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1921,949,04321,949,141

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722371alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722371Submitted genomicNC_000019.10:g.217
66241_21766339ins2
80
GRCh38 (hg38)NC_000019.10Chr1921,766,24121,766,339
nssv17722371RemappedPerfectNC_000019.9:g.2194
9043_21949141ins28
0
GRCh37.p13First PassNC_000019.9Chr1921,949,04321,949,141

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)
nssv17722371<0.00116404
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