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nsv5473801

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:172

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 133 SVs from 22 studies. See in: genome view    
Submitted genomic155,717,623-155,717,794Question Mark
Overlapping variant regions from other studies: 133 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):156,638,775-156,638,946Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473801Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4155,717,623155,717,794
nsv5473801RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4156,638,775156,638,946

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16958818deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16958818Submitted genomicNC_000004.12:g.155
717623_155717794de
l
GRCh38 (hg38)NC_000004.12Chr4155,717,623155,717,794
nssv16958818RemappedPerfectNC_000004.11:g.156
638775_156638946de
l
GRCh37.p13First PassNC_000004.11Chr4156,638,775156,638,946

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)
nssv16958818<0.00136404
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