U.S. flag

An official website of the United States government

nsv5420438

  • 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: 85 SVs from 20 studies. See in: genome view    
Submitted genomic27,409,442-27,409,493Question Mark
Overlapping variant regions from other studies: 85 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):27,420,763-27,420,814Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5420438Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1627,409,44227,409,493
nsv5420438RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1627,420,76327,420,814

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706272alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706272Submitted genomicNC_000016.10:g.274
09442_27409493ins2
81
GRCh38 (hg38)NC_000016.10Chr1627,409,44227,409,493
nssv17706272RemappedPerfectNC_000016.9:g.2742
0763_27420814ins28
1
GRCh37.p13First PassNC_000016.9Chr1627,420,76327,420,814

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)
nssv17706272<0.00116404
Support Center