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nsv4503573

  • 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: 60 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):56,627,031-56,627,031Question Mark
Overlapping variant regions from other studies: 60 SVs from 12 studies. See in: genome view    
Submitted genomic56,660,943-56,660,943Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4503573RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1656,627,03156,627,031
nsv4503573Submitted genomicGRCh37.p13Primary AssemblyNC_000016.9Chr1656,660,94356,660,943

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16014103alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16014103RemappedPerfectNC_000016.10:g.566
27031_56627032ins2
80
GRCh38.p12First PassNC_000016.10Chr1656,627,03156,627,031
nssv16014103Submitted genomicNC_000016.9:g.5666
0943_56660944ins28
0
GRCh37.p13NC_000016.9Chr1656,660,94356,660,943

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)
nssv16014103<0.001721694
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