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nsv4511028

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 41 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):33,441,047-33,441,047Question Mark
Overlapping variant regions from other studies: 41 SVs from 5 studies. See in: genome view    
Submitted genomic32,028,853-32,028,853Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4511028RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2033,441,04733,441,047
nsv4511028Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr2032,028,85332,028,853

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16033043alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16033043RemappedPerfectNC_000020.11:g.334
41047_33441048ins1
95
GRCh38.p12First PassNC_000020.11Chr2033,441,04733,441,047
nssv16033043Submitted genomicNC_000020.10:g.320
28853_32028854ins1
95
GRCh37.p13NC_000020.10Chr2032,028,85332,028,853

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)
nssv160330434.6e-005121694
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