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nsv5412243

  • 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: 76 SVs from 20 studies. See in: genome view    
Submitted genomic68,313,753-68,313,804Question Mark
Overlapping variant regions from other studies: 76 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):70,073,510-70,073,561Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5412243Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1068,313,75368,313,804
nsv5412243RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1070,073,51070,073,561

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17037419alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17037419Submitted genomicNC_000010.11:g.683
13753_68313804ins2
78
GRCh38 (hg38)NC_000010.11Chr1068,313,75368,313,804
nssv17037419RemappedPerfectNC_000010.10:g.700
73510_70073561ins2
78
GRCh37.p13First PassNC_000010.10Chr1070,073,51070,073,561

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)
nssv17037419<0.00126404
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