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nsv5486781

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:145

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 175 SVs from 24 studies. See in: genome view    
Submitted genomic142,841,256-142,841,400Question Mark
Overlapping variant regions from other studies: 175 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):143,922,672-143,922,816Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5486781Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8142,841,256142,841,400
nsv5486781RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8143,922,672143,922,816

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17018393deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17018393Submitted genomicNC_000008.11:g.142
841256_142841400de
l
GRCh38 (hg38)NC_000008.11Chr8142,841,256142,841,400
nssv17018393RemappedPerfectNC_000008.10:g.143
922672_143922816de
l
GRCh37.p13First PassNC_000008.10Chr8143,922,672143,922,816

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)
nssv17018393<0.00116404
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