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nsv5536232

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:195

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 190 SVs from 29 studies. See in: genome view    
Submitted genomic89,083,805-89,083,999Question Mark
Overlapping variant regions from other studies: 190 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):90,096,034-90,096,228Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5536232Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr889,083,80589,083,999
nsv5536232RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr890,096,03490,096,228

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17014917insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17014917Submitted genomicNC_000008.11:g.890
83805_89083999ins1
41
GRCh38 (hg38)NC_000008.11Chr889,083,80589,083,999
nssv17014917RemappedPerfectNC_000008.10:g.900
96034_90096228ins1
41
GRCh37.p13First PassNC_000008.10Chr890,096,03490,096,228

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)
nssv170149170.0492875952
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