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nsv5451171

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,935

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 347 SVs from 61 studies. See in: genome view    
Submitted genomic129,380,519-129,487,453Question Mark
Overlapping variant regions from other studies: 347 SVs from 61 studies. See in: genome view    
Remapped(Score: Perfect):129,099,362-129,206,296Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5451171Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3129,380,519129,487,453
nsv5451171RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3129,099,362129,206,296

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16939162deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16939162Submitted genomicNC_000003.12:g.129
380519_129487453de
l
GRCh38 (hg38)NC_000003.12Chr3129,380,519129,487,453
nssv16939162RemappedPerfectNC_000003.11:g.129
099362_129206296de
l
GRCh37.p13First PassNC_000003.11Chr3129,099,362129,206,296

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)
nssv16939162<0.00116404
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