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nsv4458939

  • 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: 23 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):151,714,775-151,714,775Question Mark
Overlapping variant regions from other studies: 25 SVs from 6 studies. See in: genome view    
Submitted genomic151,687,251-151,687,251Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4458939RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1151,714,775151,714,775
nsv4458939Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1151,687,251151,687,251

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16028640alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16028640RemappedPerfectNC_000001.11:g.151
714775_151714776in
s280
GRCh38.p12First PassNC_000001.11Chr1151,714,775151,714,775
nssv16028640Submitted genomicNC_000001.10:g.151
687251_151687252in
s280
GRCh37.p13NC_000001.10Chr1151,687,251151,687,251

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)
nssv160286404.6e-005121694
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