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nsv5418334

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 193 SVs from 22 studies. See in: genome view    
Submitted genomic129,889,647-129,889,647Question Mark
Overlapping variant regions from other studies: 193 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):129,759,542-129,759,542Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5418334Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11129,889,647129,889,647
nsv5418334RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11129,759,542129,759,542

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052684alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052684Submitted genomicNC_000011.10:g.129
889647_129889648in
s289
GRCh38 (hg38)NC_000011.10Chr11129,889,647129,889,647
nssv17052684RemappedPerfectNC_000011.9:g.1297
59542_129759543ins
289
GRCh37.p13First PassNC_000011.9Chr11129,759,542129,759,542

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)
nssv170526840.29717705960
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