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nsv5476356

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,578

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 238 SVs from 34 studies. See in: genome view    
Submitted genomic124,453,346-124,461,923Question Mark
Overlapping variant regions from other studies: 238 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):125,465,587-125,474,164Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5476356Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8124,453,346124,461,923
nsv5476356RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8125,465,587125,474,164

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17017109deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17017109Submitted genomicNC_000008.11:g.124
453346_124461923de
l
GRCh38 (hg38)NC_000008.11Chr8124,453,346124,461,923
nssv17017109RemappedPerfectNC_000008.10:g.125
465587_125474164de
l
GRCh37.p13First PassNC_000008.10Chr8125,465,587125,474,164

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)
nssv17017109<0.00116404
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