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nsv4483279

  • 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: 37 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):56,499,270-56,499,270Question Mark
Overlapping variant regions from other studies: 37 SVs from 5 studies. See in: genome view    
Submitted genomic57,411,829-57,411,829Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4483279RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr856,499,27056,499,270
nsv4483279Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr857,411,82957,411,829

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16080045alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16080045RemappedPerfectNC_000008.11:g.564
99270_56499271ins2
81
GRCh38.p12First PassNC_000008.11Chr856,499,27056,499,270
nssv16080045Submitted genomicNC_000008.10:g.574
11829_57411830ins2
81
GRCh37.p13NC_000008.10Chr857,411,82957,411,829

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)
nssv160800454.6e-005121694
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