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nsv4541484

  • 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: 40 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):102,523,620-102,523,620Question Mark
Overlapping variant regions from other studies: 40 SVs from 8 studies. See in: genome view    
Submitted genomic102,394,351-102,394,351Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4541484RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11102,523,620102,523,620
nsv4541484Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr11102,394,351102,394,351

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15997411insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15997411RemappedPerfectNC_000011.10:g.102
523620_102523621in
s317
GRCh38.p12First PassNC_000011.10Chr11102,523,620102,523,620
nssv15997411Submitted genomicNC_000011.9:g.1023
94351_102394352ins
317
GRCh37.p13NC_000011.9Chr11102,394,351102,394,351

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)
nssv15997411<0.001621694
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