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nsv4162691

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,362

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):114,067,086-114,068,447Question Mark
Overlapping variant regions from other studies: 96 SVs from 15 studies. See in: genome view    
Submitted genomic115,079,315-115,080,676Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4162691RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8114,067,086114,068,447
nsv4162691Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr8115,079,315115,080,676

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15928560deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15928560RemappedPerfectNC_000008.11:g.114
067086_114068447de
l
GRCh38.p12First PassNC_000008.11Chr8114,067,086114,068,447
nssv15928560Submitted genomicNC_000008.10:g.115
079315_115080676de
l
GRCh37.p13NC_000008.10Chr8115,079,315115,080,676

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)
nssv159285600.131284421692
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