nsv4459118

  • 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: 29 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):150,513,583-150,513,583Question Mark
Overlapping variant regions from other studies: 32 SVs from 7 studies. See in: genome view    
Submitted genomic150,486,059-150,486,059Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4459118RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1150,513,583150,513,583
nsv4459118Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1150,486,059150,486,059

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16027560alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16027560RemappedPerfectNC_000001.11:g.150
513583_150513584in
s121
GRCh38.p12First PassNC_000001.11Chr1150,513,583150,513,583
nssv16027560Submitted genomicNC_000001.10:g.150
486059_150486060in
s121
GRCh37.p13NC_000001.10Chr1150,486,059150,486,059

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)
nssv160275604.6e-005121694
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