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nsv5450691

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,762

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 24 studies. See in: genome view    
Submitted genomic231,979,353-231,983,114Question Mark
Overlapping variant regions from other studies: 108 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):232,844,063-232,847,824Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5450691Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2231,979,353231,983,114
nsv5450691RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2232,844,063232,847,824

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928589deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928589Submitted genomicNC_000002.12:g.231
979353_231983114de
l
GRCh38 (hg38)NC_000002.12Chr2231,979,353231,983,114
nssv16928589RemappedPerfectNC_000002.11:g.232
844063_232847824de
l
GRCh37.p13First PassNC_000002.11Chr2232,844,063232,847,824

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)
nssv16928589<0.00166404
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