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nsv5450165

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 185 SVs from 39 studies. See in: genome view    
Submitted genomic131,617,562-131,617,632Question Mark
Overlapping variant regions from other studies: 185 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):132,375,135-132,375,205Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5450165Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2131,617,562131,617,632
nsv5450165RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2132,375,135132,375,205

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16917847duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16917847Submitted genomicNC_000002.12:g.131
617562_131617632du
p
GRCh38 (hg38)NC_000002.12Chr2131,617,562131,617,632
nssv16917847RemappedPerfectNC_000002.11:g.132
375135_132375205du
p
GRCh37.p13First PassNC_000002.11Chr2132,375,135132,375,205

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)
nssv16917847<0.00126404
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