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nsv5453150

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:109

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 34 studies. See in: genome view    
Submitted genomic184,720,513-184,720,621Question Mark
Overlapping variant regions from other studies: 164 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):184,689,647-184,689,755Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5453150Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1184,720,513184,720,621
nsv5453150RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1184,689,647184,689,755

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892895deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892895Submitted genomicNC_000001.11:g.184
720513_184720621de
l
GRCh38 (hg38)NC_000001.11Chr1184,720,513184,720,621
nssv16892895RemappedPerfectNC_000001.10:g.184
689647_184689755de
l
GRCh37.p13First PassNC_000001.10Chr1184,689,647184,689,755

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)
nssv168928950.012806402
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