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nsv5400157

  • 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: 97 SVs from 22 studies. See in: genome view    
Submitted genomic63,885,478-63,885,529Question Mark
Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):63,871,154-63,871,205Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400157Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr363,885,47863,885,529
nsv5400157RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr363,871,15463,871,205

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933897alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933897Submitted genomicNC_000003.12:g.638
85478_63885529ins2
80
GRCh38 (hg38)NC_000003.12Chr363,885,47863,885,529
nssv16933897RemappedPerfectNC_000003.11:g.638
71154_63871205ins2
80
GRCh37.p13First PassNC_000003.11Chr363,871,15463,871,205

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)
nssv16933897<0.00116404
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