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nsv5401063

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 155 SVs from 37 studies. See in: genome view    
Submitted genomic73,130,279-73,130,330Question Mark
Overlapping variant regions from other studies: 155 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):73,995,996-73,996,047Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5401063Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr473,130,27973,130,330
nsv5401063RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr473,995,99673,996,047

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952227alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952227Submitted genomicNC_000004.12:g.731
30279_73130330ins2
81
GRCh38 (hg38)NC_000004.12Chr473,130,27973,130,330
nssv16952227RemappedPerfectNC_000004.11:g.739
95996_73996047ins2
81
GRCh37.p13First PassNC_000004.11Chr473,995,99673,996,047

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)
nssv16952227<0.00126404
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