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nsv5401633

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 20 studies. See in: genome view    
Submitted genomic56,671,600-56,671,651Question Mark
Overlapping variant regions from other studies: 113 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):57,137,273-57,137,324Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5401633Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr156,671,60056,671,651
nsv5401633RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr157,137,27357,137,324

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16903042alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16903042Submitted genomicNC_000001.11:g.566
71600_56671651ins2
65
GRCh38 (hg38)NC_000001.11Chr156,671,60056,671,651
nssv16903042RemappedPerfectNC_000001.10:g.571
37273_57137324ins2
65
GRCh37.p13First PassNC_000001.10Chr157,137,27357,137,324

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)
nssv16903042<0.00126404
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