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nsv5463183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,490

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 369 SVs from 42 studies. See in: genome view    
Submitted genomic186,524,299-186,530,788Question Mark
Overlapping variant regions from other studies: 369 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):187,445,453-187,451,942Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5463183Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4186,524,299186,530,788
nsv5463183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4187,445,453187,451,942

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16962316deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16962316Submitted genomicNC_000004.12:g.186
524299_186530788de
l
GRCh38 (hg38)NC_000004.12Chr4186,524,299186,530,788
nssv16962316RemappedPerfectNC_000004.11:g.187
445453_187451942de
l
GRCh37.p13First PassNC_000004.11Chr4187,445,453187,451,942

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)
nssv16962316<0.00116404
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