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nsv5549192

  • 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: 149 SVs from 32 studies. See in: genome view    
Submitted genomic21,933,009-21,933,009Question Mark
Overlapping variant regions from other studies: 149 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):22,085,943-22,085,943Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5549192Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1221,933,00921,933,009
nsv5549192RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1222,085,94322,085,943

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17688495insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17688495Submitted genomicNC_000012.12:g.219
33009_21933010ins3
34
GRCh38 (hg38)NC_000012.12Chr1221,933,00921,933,009
nssv17688495RemappedPerfectNC_000012.11:g.220
85943_22085944ins3
34
GRCh37.p13First PassNC_000012.11Chr1222,085,94322,085,943

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)
nssv176884950.33320866258
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