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nsv5484687

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,881

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 159 SVs from 15 studies. See in: genome view    
Submitted genomic135,532,279-135,534,159Question Mark
Overlapping variant regions from other studies: 159 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):136,544,522-136,546,402Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5484687Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8135,532,279135,534,159
nsv5484687RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8136,544,522136,546,402

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17019788deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17019788Submitted genomicNC_000008.11:g.135
532279_135534159de
l
GRCh38 (hg38)NC_000008.11Chr8135,532,279135,534,159
nssv17019788RemappedPerfectNC_000008.10:g.136
544522_136546402de
l
GRCh37.p13First PassNC_000008.10Chr8136,544,522136,546,402

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)
nssv17019788<0.00116404
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