nsv5414438

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,141

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 93 SVs from 26 studies. See in: genome view    
Submitted genomic33,148,847-33,150,987Question Mark
Overlapping variant regions from other studies: 93 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):33,614,448-33,616,588Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414438Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr133,148,84733,150,987
nsv5414438RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr133,614,44833,616,588

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901390deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901390Submitted genomicNC_000001.11:g.331
48847_33150987del
GRCh38 (hg38)NC_000001.11Chr133,148,84733,150,987
nssv16901390RemappedPerfectNC_000001.10:g.336
14448_33616588del
GRCh37.p13First PassNC_000001.10Chr133,614,44833,616,588

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)
nssv16901390<0.00126404
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