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nsv4322188

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:912

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):15,492,650-15,493,561Question Mark
Overlapping variant regions from other studies: 112 SVs from 8 studies. See in: genome view    
Submitted genomic15,350,159-15,351,070Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4322188RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr815,492,65015,493,561
nsv4322188Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr815,350,15915,351,070

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091436inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091436RemappedPerfectNC_000008.11:g.154
92650_15493561inv
GRCh38.p12First PassNC_000008.11Chr815,492,65015,493,561
nssv16091436Submitted genomicNC_000008.10:g.153
50159_15351070inv
GRCh37.p13NC_000008.10Chr815,350,15915,351,070

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)
nssv16091436<0.001421686
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